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!DOCTYPE html>html langen>head>    title>        Home - Neomorph    /title>    meta charsetutf-8>meta nameviewport contentwidthdevice-width, initial-scale1>link relshortcut icon href./images/favicon.ico typeimage/png />link relicon href./images/favicon.ico typeimage/png />link relstylesheet hrefhttps://use.typekit.net/xgu7mnt.css>link relstylesheet href./css/styles.css />script src./vendor/jquery/jquery.min.js>/script>script src./vendor/bootstrap/js/bootstrap.min.js>/script>script srchttps://www.google.com/recaptcha/api.js>/script>script src./settings/settings.js>/script>script src./js/scripts.js>/script>!-- Global site tag (gtag.js) - Google Analytics -->script>    $(head).append(`script async srchttps://www.googletagmanager.com/gtag/js?id${settings.GtagId}>` + /script>)    window.dataLayer  window.dataLayer || ;    function gtag(){dataLayer.push(arguments);}    gtag(js, new Date());    gtag(config, settings.GtagId);/script>/head>body>div idheader>    div classmobile-nav-menu>        div classmobile-nav-item bot-border onclickmobileChangePage(about)>About/div>        div classmobile-nav-item bot-border onclickmobileChangePage(science)>Science/div>        div classmobile-nav-item bot-border onclickmobileChangePage(news)>News/div>        div classmobile-nav-item bot-border onclickmobileChangePage(leadership)>Leadership/div>        div classmobile-nav-item bot-border onclickmobileChangePage(careers)>Careers/div>!--        div classmobile-nav-item bot-border>a hrefhttps://careers-neomorph.icims.com/>Careers/a>/div>-->        div classmobile-nav-item bot-border onclickmobileChangePage(contact)>Contact/div>        div classmobile-nav-item bot-border>a hrefprivacy.html>Privacy Policy/a>/div>        div classmobile-nav-item bot-border>a hrefterms.html>Terms/a>/div>        div classmobile-nav-item bot-border>            a target_blank hrefhttps://www.linkedin.com/company/neomorph-llc>img stylewidth:30px; 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   })/script>div classbody-content>    !-- The video -->    div idbg>        video autoplay muted loop idmyVideo>            source srcimages/video/D15_110820_draw1_edited.mp4 typevideo/mp4>        /video>    /div>    div idSearchWrapper classfade-in-delayed>        img srcimages/header/magnifying glass-blue.png classmagnifying-glass />        input typetext/>    /div>    main classwrapper>        !-- Landing page -->        div classhome-content tagline screen idhome>    div classhome-img-placeholder>    /div>    div classhome-img-wrapper>        div classleft-img styleopacity: 0>            img srcimages/home/Home-left-image-odl.png height3017 width3038/>        /div>        div classcenter-img styleopacity: 0>            img srcimages/home/Home-center-image-old.png height3017 width3038/>        /div>        div classright-img styleopacity: 0>            img srcimages/home/Home-right-image-old.png height3017 width3038/>        /div>        div classtransition-img styleopacity: 0>            img srcimages/header/neomorph-icon-color-02.png height538 width343/>        /div>    /div>    div classhome-text-wrapper styleopacity: 0>        p classhome-title>NEOMORPH/p>        div classhome-text-bottom-half>            p classhome-text>                Advancing the science of targeted protein degradation to destroy ‘undruggable’ proteins and cure disease            /p>            div classscroll-button>                !--div classarrow-line>-->                !--/div>-->                div classarrow-bottom>                    svg width60 height30 viewBox-2.5 -5 75 60 preserveAspectRationone>                        path dM0,0 l35,50 l35,-50 fillnone stroke#2A3972 stroke-linecapround stroke-width5>/path>                    /svg>                /div>            /div>        /div>    /div>/div>        !-- About page -->        div classabout-content screen hidden idabout>    div classabout-header>        h1>About/h1>    /div>    div classabout-paragraph>        p>            Neomorph is a venture backed biotechnology company solving critical problems in human health through the discovery and development of innovative new medicines against ‘undruggable targets’. Our team is comprised of industry leading experts in protein degradation and molecular glues who have a track record of ground-breaking discoveries in the field. We are committed to leadership in advancing the science and technology of molecular glue drug discovery, while prosecuting a pipeline of projects through clinical development. Our patient-first, science-driven approach is complemented by our dedication to a supportive and collaborative work environment. Neomorph is headquartered in San Diego, California.        /p>    /div>/div>        !-- Science page -->        div classscience-content screen hidden idscience>    div classscience-header>        h1>Science/h1>    /div>    div classscience-paragraph>        p classscience-title>            Targeted Protein Degradation Therapeutic Discovery        /p>        p>            Targeted protein degradation drugs work by repurposing the cellular machinery to destroy proteins linked to disease. Some degraders work by redirecting cellular machines known as E3 ubiquitin ligases to disease-causing proteins, causing them to be marked for degradation. These degraders can be classified as heterobifunctional (e.g. PROTACs) or ‘molecular glue’ (e.g. indisulam or thalidomide). There has been an explosion of interest in targeted protein degradation in recent years due to the convergence of two advances: heterobifunctional molecules were optimized to be suitable for i>in vivo/i> use, and clinically approved drugs were found to function via the ‘molecular glue’ degradation mechanism. Together, these scientific advances offer an opportunity to tackle targets and diseases that had been considered intractable to conventional drug discovery.        /p>        p classscience-title>            Molecular Glue As A Solution to ‘Undruggable’ Targets        /p>        p>            Historically, conventional therapeutics fell into the categories of large and small molecule drugs, with large molecules such as antibodies able to target extracellular targets, and small molecules able to target extracellular or intracellular targets. Small molecule campaigns are typically limited to targets shown to be ‘druggable’. Druggable targets have a binding pocket that can support high-affinity binding to a drug molecule with appropriate properties for clinical use. Binding alone is often insufficient to achieve a biological effect, so drug binding in the pocket must also perturb cellular biology in a way that is clinically beneficial. However, many disease-causing proteins lack druggable binding pockets, or drug binding alone does not cause the desired biological effect, and these targets have been considered ‘undruggable’. Targeted protein degradation offers a path to solving this problem by triggering the destruction of the target protein by the 26S proteasome, thereby removing all of the associated biological activities. While heterobifunctional drugs still require a druggable binding pocket on the target protein, molecular glue drugs are able to bypass this requirement, and as such offer a differentiated approach to drug discovery with different rules and the potential to target a broad section of the proteome. Molecular glue drugs have been described relatively recently, but the science is now well-established and the therapeutic mechanism has been clinically validated through an understanding of the recruitment of neomorphic substrates to CRL4sup>CRBN/sup> by thalidomide analogs, as well as the recruitment of RBM39 to CRL4sup>DCAF15/sup> by indisulam.        /p>        p classscience-title>            Further Reading        /p>        span classfurtherReading>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/24292625/>Lenalidomide causes selective degradation of IKZF1 and IKZF3 in multiple myeloma cells. Krönke J, Udeshi ND, Narla A, Grauman P, Hurst SN, McConkey M, Svinkina T, Heckl D, Comer E, Li X, Ciarlo C, Hartman E, Munshi N, Schenone M, Schreiber SL, Carr SA, Ebert BL. Science. 2014 Jan 17;343(6168):301-5. doi: 10.1126/science.1244851. Epub 2013 Nov 29. PMID: 24292625; PMCID: PMC4077049.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/24292623/>The myeloma drug lenalidomide promotes the cereblon-dependent destruction of Ikaros proteins.Lu G, Middleton RE, Sun H, Naniong M, Ott CJ, Mitsiades CS, Wong KK, Bradner JE, Kaelin WG Jr. Science. 2014 Jan 17;343(6168):305-9. doi: 10.1126/science.1244917. Epub 2013 Nov 29. PMID: 24292623; PMCID: PMC4070318.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/24328678/>Immunomodulatory agents lenalidomide and pomalidomide co-stimulate T cells by inducing degradation of T cell repressors Ikaros and Aiolos via modulation of the E3 ubiquitin ligase complex CRL4(CRBN.). Gandhi AK, Kang J, Havens CG, Conklin T, Ning Y, Wu L, Ito T, Ando H, Waldman MF, Thakurta A, Klippel A, Handa H, Daniel TO, Schafer PH, Chopra R. Br J Haematol. 2014 Mar;164(6):811-21. doi: 10.1111/bjh.12708. Epub 2013 Dec 13. PMID: 24328678; PMCID: PMC4232904.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/25043012/>Structure of the DDB1-CRBN E3 ubiquitin ligase in complex with thalidomide. Fischer ES, Böhm K, Lydeard JR, Yang H, Stadler MB, Cavadini S, Nagel J, Serluca F, Acker V, Lingaraju GM, Tichkule RB, Schebesta M, Forrester WC, Schirle M, Hassiepen U, Ottl J, Hild M, Beckwith RE, Harper JW, Jenkins JL, Thomä NH. Nature. 2014 Aug 7;512(7512):49-53. doi: 10.1038/nature13527. Epub 2014 Jul 16. PMID: 25043012; PMCID: PMC4423819.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/25108355/>Structure of the human Cereblon-DDB1-lenalidomide complex reveals basis for responsiveness to thalidomide analogs. Chamberlain PP, Lopez-Girona A, Miller K, Carmel G, Pagarigan B, Chie-Leon B, Rychak E, Corral LG, Ren YJ, Wang M, Riley M, Delker SL, Ito T, Ando H, Mori T, Hirano Y, Handa H, Hakoshima T, Daniel TO, Cathers BE. Nat Struct Mol Biol. 2014 Sep;21(9):803-9. doi: 10.1038/nsmb.2874. Epub 2014 Aug 10. PMID: 25108355.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/26131937/>Lenalidomide induces ubiquitination and degradation of CK1α in del(5q) MDS. Krönke J, Fink EC, Hollenbach PW, MacBeth KJ, Hurst SN, Udeshi ND, Chamberlain PP, Mani DR, Man HW, Gandhi AK, Svinkina T, Schneider RK, McConkey M, Järås M, Griffiths E, Wetzler M, Bullinger L, Cathers BE, Carr SA, Chopra R, Ebert BL. Nature. 2015 Jul 9;523(7559):183-188. doi: 10.1038/nature14610. Epub 2015 Jul 1. PMID: 26131937; PMCID: PMC4853910.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/26909574/>Structural basis of lenalidomide-induced CK1α degradation by the CRL4(CRBN) ubiquitin ligase. Petzold G, Fischer ES, Thomä NH. Nature. 2016 Apr 7;532(7597):127-30. doi: 10.1038/nature16979. Epub 2016 Feb 24. PMID: 26909574.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/27338790/>A novel cereblon modulator recruits GSPT1 to the CRL4(CRBN) ubiquitin ligase. Matyskiela ME, Lu G, Ito T, Pagarigan B, Lu CC, Miller K, Fang W, Wang NY, Nguyen D, Houston J, Carmel G, Tran T, Riley M, Nosaka L, Lander GC, Gaidarova S, Xu S, Ruchelman AL, Handa H, Carmichael J, Daniel TO, Cathers BE, Lopez-Girona A, Chamberlain PP. Nature. 2016 Jul 14;535(7611):252-7. doi: 10.1038/nature18611. Epub 2016 Jun 22. PMID: 27338790.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/28530236/>pSILAC mass spectrometry reveals ZFP91 as IMiD-dependent substrate of the CRL4sup>CRBN/sup> ubiquitin ligase. An J, Ponthier CM, Sack R, Seebacher J, Stadler MB, Donovan KA, Fischer ES. Nat Commun. 2017 May 22;8:15398. doi: 10.1038/ncomms15398. PMID: 28530236; PMCID: PMC5458144.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/28425720/>A Cereblon Modulator (CC-220) with Improved Degradation of Ikaros and Aiolos. Matyskiela ME, Zhang W, Man HW, Muller G, Khambatta G, Baculi F, Hickman M, LeBrun L, Pagarigan B, Carmel G, Lu CC, Lu G, Riley M, Satoh Y, Schafer P, Daniel TO, Carmichael J, Cathers BE, Chamberlain PP. J Med Chem. 2018 Jan 25;61(2):535-542. doi: 10.1021/acs.jmedchem.6b01921. Epub 2017 Apr 20. PMID: 28425720.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/28302793/>Anticancer sulfonamides target splicing by inducing RBM39 degradation via recruitment to DCAF15. Han T, Goralski M, Gaskill N, Capota E, Kim J, Ting TC, Xie Y, Williams NS, Nijhawan D. Science. 2017 Apr 28;356(6336):eaal3755. doi: 10.1126/science.aal3755. Epub 2017 Mar 16. Erratum in: Science. 2017 May 26;356(6340):null. PMID: 28302793.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/28437394/>Selective degradation of splicing factor CAPERα by anticancer sulfonamides. Uehara T, Minoshima Y, Sagane K, Sugi NH, Mitsuhashi KO, Yamamoto N, Kamiyama H, Takahashi K, Kotake Y, Uesugi M, Yokoi A, Inoue A, Yoshida T, Mabuchi M, Tanaka A, Owa T. Nat Chem Biol. 2017 Jun;13(6):675-680. doi: 10.1038/nchembio.2363. Epub 2017 Apr 24. PMID: 28437394.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/30067223/>Thalidomide promotes degradation of SALL4, a transcription factor implicated in Duane Radial Ray syndrome. Donovan KA, An J, Nowak RP, Yuan JC, Fink EC, Berry BC, Ebert BL, Fischer ES. Elife. 2018 Aug 1;7:e38430. doi: 10.7554/eLife.38430. PMID: 30067223; PMCID: PMC6156078.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/30042095/>Genome-wide screen identifies cullin-RING ligase machinery required for lenalidomide-dependent CRL4sup>CRBN/sup> activity. Sievers QL, Gasser JA, Cowley GS, Fischer ES, Ebert BL. Blood. 2018 Sep 20;132(12):1293-1303. doi: 10.1182/blood-2018-01-821769. Epub 2018 Jul 24. PMID: 30042095; PMCID: PMC6148446.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/30234487/>UBE2G1 governs the destruction of cereblon neomorphic substrates. Lu G, Weng S, Matyskiela M, Zheng X, Fang W, Wood S, Surka C, Mizukoshi R, Lu CC, Mendy D, Jang IS, Wang K, Marella M, Couto S, Cathers B, Carmichael J, Chamberlain P, Rolfe M. Elife. 2018 Sep 20;7:e40958. doi: 10.7554/eLife.40958. PMID: 30234487; PMCID: PMC6185104.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/30190590/>SALL4 mediates teratogenicity as a thalidomide-dependent cereblon substrate. Matyskiela ME, Couto S, Zheng X, Lu G, Hui J, Stamp K, Drew C, Ren Y, Wang M, Carpenter A, Lee CW, Clayton T, Fang W, Lu CC, Riley M, Abdubek P, Blease K, Hartke J, Kumar G, Vessey R, Rolfe M, Hamann LG, Chamberlain PP. Nat Chem Biol. 2018 Oct;14(10):981-987. doi: 10.1038/s41589-018-0129-x. Epub 2018 Sep 6. PMID: 30190590.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/30064974/>Crbnsup>I391V/sup> is sufficient to confer in vivo sensitivity to thalidomide and its derivatives in mice. Fink EC, McConkey M, Adams DN, Haldar SD, Kennedy JA, Guirguis AA, Udeshi ND, Mani DR, Chen M, Liddicoat B, Svinkina T, Nguyen AT, Carr SA, Ebert BL.  Blood. 2018 Oct 4;132(14):1535-1544. doi: 10.1182/blood-2018-05-852798. Epub 2018 Jul 31. PMID: 30064974; PMCID: PMC6172563.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/30385546/>Defining the human C2H2 zinc finger degrome targeted by thalidomide analogs through CRBN. Sievers QL, Petzold G, Bunker RD, Renneville A, Słabicki M, Liddicoat BJ, Abdulrahman W, Mikkelsen T, Ebert BL, Thomä NH. Science. 2018 Nov 2;362(6414):eaat0572. doi: 10.1126/science.aat0572. PMID: 30385546; PMCID: PMC6326779.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/31527835/>Development of targeted protein degradation therapeutics. Chamberlain PP, Hamann LG. Nat Chem Biol. 2019 Oct;15(10):937-944. doi: 10.1038/s41589-019-0362-y. Epub 2019 Sep 16. PMID: 31527835.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/31693911/>Structural Basis and Kinetic Pathway of RBM39 Recruitment to DCAF15 by a Sulfonamide Molecular Glue E7820. Du X, Volkov OA, Czerwinski RM, Tan H, Huerta C, Morton ER, Rizzi JP, Wehn PM, Xu R, Nijhawan D, Wallace EM. Structure. 2019 Nov 5;27(11):1625-1633.e3. doi: 10.1016/j.str.2019.10.005. PMID: 31693911.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/31857833/>Evolution of Cereblon-Mediated Protein Degradation as a Therapeutic Modality. Chamberlain PP, DAgostino LA, Ellis JM, Hansen JD, Matyskiela ME, McDonald JJ, Riggs JR, Hamann LG. ACS Med Chem Lett. 2019 Nov 12;10(12):1592-1602. doi: 10.1021/acsmedchemlett.9b00425. PMID: 31857833; PMCID: PMC6912861.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/31819272/>Structural basis of indisulam-mediated RBM39 recruitment to DCAF15 E3 ligase complex. Bussiere DE, Xie L, Srinivas H, Shu W, Burke A, Be C, Zhao J, Godbole A, King D, Karki RG, Hornak V, Xu F, Cobb J, Carte N, Frank AO, Frommlet A, Graff P, Knapp M, Fazal A, Okram B, Jiang S, Michellys PY, Beckwith R, Voshol H, Wiesmann C, Solomon JM, Paulk J. Nat Chem Biol. 2020 Jan;16(1):15-23. doi: 10.1038/s41589-019-0411-6. Epub 2019 Dec 9. 16(3):361. PMID: 31819272.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/31686031/>Structural complementarity facilitates E7820-mediated degradation of RBM39 by DCAF15.  Faust TB, Yoon H, Nowak RP, Donovan KA, Li Z, Cai Q, Eleuteri NA, Zhang T, Gray NS, Fischer ES. Nat Chem Biol. 2020 Jan;16(1):7-14. doi: 10.1038/s41589-019-0378-3. Epub 2019 Nov 4. PMID: 31686031; PMCID: PMC6917914.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/32251415/>Crystal structure of the SALL4-pomalidomide-cereblon-DDB1 complex. Matyskiela ME, Clayton T, Zheng X, Mayne C, Tran E, Carpenter A, Pagarigan B, McDonald J, Rolfe M, Hamann LG, Lu G, Chamberlain PP. Nat Struct Mol Biol. 2020 Apr;27(4):319-322. doi: 10.1038/s41594-020-0405-9. Epub 2020 Apr 6. PMID: 32251415.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubmed.ncbi.nlm.nih.gov/32494016/>The CDK inhibitor CR8 acts as a molecular glue degrader that depletes cyclin K. Słabicki M, Kozicka Z, Petzold G, Li YD, Manojkumar M, Bunker RD, Donovan KA, Sievers QL, Koeppel J, Suchyta D, Sperling AS, Fink EC, Gasser JA, Wang LR, Corsello SM, Sellar RS, Jan M, Gillingham D, Scholl C, Fröhling S, Golub TR, Fischer ES, Thomä NH, Ebert BL. Nature. 2020 Sep;585(7824):293-297. doi: 10.1038/s41586-020-2374-x. Epub 2020 Jun 3. PMID: 32494016; PMCID: PMC7486275.                    /a>                /p>                p>                    a classscience-link hrefhttps://pubs.rsc.org/en/content/chapter/9781839160691-00094/978-1-83916-069-1>Chapter 5: New Activities of CELMoDs, Cereblon E3 Ligase Modulating Drugs. Matyskiela ME, Clayton T, Thompson J, Carroll C, Bateman L, LeBrun L, Chamberlain PP. Protein Degradation with New Chemical Modalities: Successful Strategies in Drug Discovery and Chemical Biology. The Royal Society of Chemistry publications. 2020 Oct 8. doi: 10.1039/9781839160691-00094.                    /a>                /p>                /span>    /div>/div>        !-- News page -->        div classnews-content screen hidden idnews>    div classnews-header idnewsHeader>        h1>News/h1>    /div>    div classnews-article-section>        div idnewsArticles classnews-articles>            div classnews-article-title>                a hrefhttps://www.linkedin.com/feed/update/urn:li:activity:7424515604423995393 target_blank stylecolor: #2a3972;>                    Neomorph Announces First Patient Dosed in Phase 1/2 Trial Evaluating NEO-811 in ccRCC                /a>                div classnews-article-date>                    February 3, 2026 at 1:00 pm ET                    br>a hrefimages/news/Neomorph_FPD_Press_Release.pdf target_blank>Click here/a> for Press Release                    p classmt-3>                        a hrefhttps://www.linkedin.com/feed/update/urn:li:activity:7424515604423995393 target_blank>                            Hear From Our Co-Founder, President, and CEO Phil Chamberlain, DPhil. and CMO Klaus                             br classd-none d-xl-block/>                            Wagner, MD, PhD on What This Milestone Means For Patients and The Future of Our Platform                        /a>                    /p>                /div>                     /div>            separator>/separator>            div classnews-article-title>                Neomorph and AbbVie Announce Collaboration                div classnews-article-date>                    January 23, 2025 at 9:00 am ET                    br>a hrefimages/news/AbbVie-Neomorph.pdf target_blank>Click here/a> for Press Release                /div>                         /div>            separator>/separator>            div classnews-article-title>                Neomorph Announces Appointment of Dr. Klaus Wagner, M.D., Ph.D. as Chief Medical Officer                div classnews-article-date>                    January 14, 2025 at 9:00 am ET                    br>a hrefhttps://us-east-2.protection.sophos.com/?dprnewswire.com&uaHR0cHM6Ly93d3cucHJuZXdzd2lyZS5jb20vbmV3cy1yZWxlYXNlcy9uZW9tb3JwaC1hbm5vdW5jZXMtYXBwb2ludG1lbnQtb2YtZHIta2xhdXMtd2FnbmVyLW1kLXBoZC1hcy1jaGllZi1tZWRpY2FsLW9mZmljZXItMzAyMzUwMjExLmh0bWw_dGM9ZW1sX2NsZWFydGltZQ&iNjJiZjRmZWQ1YTVmZjgxMTRhYjE2NjFk&tTU9iUG9kUmF3UFNnU1V4ZGY5akZNcWZqRXZUMTM3UzRQaHd1T2VzYkRLOD0&hb65cca754d7f42e2b533e77ec81c7820&sAVNPUEhUT0NFTkNSWVBUSVZyWiwIqGd2hNRHG8bSotaTta6nvGFaRW8lvpswW4_kUg target_blank>Click here/a> for Press Release                /div>                            /div>            separator>/separator>            div classnews-article-title>                Neomorph and Biogen Announce Research Collaboration                div classnews-article-date>                    October 29, 2024 at 6:00pm ET                /div>                div classnews-read-more news-link-styling onclicknewsReadMore(this) data-articlearticle6>                    span classnews-click-here>Click here/span> for Press Release                /div>            /div>            separator>/separator>            div classnews-article-title>                img srcimages/leadership/peter-lebowitz.png />                Neomorph Announces Appointment of Dr. Peter Lebowitz, M.D., Ph.D. to its Board of Directors                div classnews-article-date>                    August 20th, 2024 at 9:00am ET                    br>a hrefhttps://www.prnewswire.com/news-releases/neomorph-announces-appointment-of-dr-peter-lebowitz-md-phd-to-its-board-of-directors-302225853.html target_blank>Click here/a> for Press Release                /div>            /div>            separator>/separator>            div classnews-article-title>                Neomorph Announces Discovery Collaboration with Novo Nordisk                div classnews-article-date>                    February 26, 2024 at 12:00pm ET                /div>                div classnews-read-more news-link-styling onclicknewsReadMore(this) data-articlearticle5>                    span classnews-click-here>Click here/span> for Press Release                /div>            /div>            separator>/separator>            div classnews-article-title>                img srcimages/leadership/Bell_Zhong.png/>                Bell Zhong Named as Chief Financial Officer of Neomorph                div classnews-article-date>                    September 7th, at 12:00pm ET                    br>a classnews-click-here hrefhttps://lnkd.in/giMHbU6m target_blank>Click here/a> for Business Wire Article                /div>            /div>            separator>/separator>            div classnews-article-title>                img srcimages/news/PhilC_new.png/>                Guggenheim Healthcare Talks - Targeted Protein Degradation Day                div classnews-article-date>                    March 16, 2022, at 3:30pm ET                    br>a classnews-click-here hrefhttps://kvgo.com/guggenheim/neomorph-march-2022 target_blank>Click here for Webcast/a>                /div>            /div>            separator>/separator>            div classnews-article-title>                img srcimages/news/PhilC_new.png/>                Neomorph Inc., to Participate in Upcoming Guggenheim Healthcare Talks - Targeted Protein Degradation Day                div classnews-article-date>                    March 10th, 2022                /div>                div classnews-read-more onclicknewsReadMore(this) data-articlearticle3>                    Read More                /div>            /div>            separator>/separator>            div classnews-article-title>                img srcimages/news/phil_2.png/>                Philip Chamberlain Named as Chief Executive Officer of Neomorph                div classnews-article-date>                    November 29th, 2021                /div>                div classnews-read-more onclicknewsReadMore(this) data-articlearticle2>                    Read More                /div>            /div>            separator>/separator>            div classnews-article-title>                img srcimages/news/Neomorph_building1x.png/>                Neomorph, Inc. Announces $109 Million Series A Financing br>to Advance Proprietary Protein Degradation Platform and Programs                div classnews-article-date>                    December 20th, 2020                /div>                div classnews-read-more onclicknewsReadMore(this) data-articlearticle1>                    Read More                /div>            /div>        /div>        div classnews-article-wrapper>            div classnews-back-button onclicknewsBackClick()>            /div>            div classnews-article idarticle1 styledisplay:none;>                h2>a target_blank hrefhttps://www.businesswire.com/news/home/20201222005199/en/Neomorph-Inc.-Announces-109-Million-Series-A-Financing-to-Advance-Proprietary-Protein-Degradation-Platform-and-Programs>                    Neomorph, Inc. Announces $109 Million Series A Financing to Advance Proprietary Protein Degradation Platform and Programs                /a>/h2>                p>b>(San Diego, CA, December 20th, 2020)—/b>/b>Neomorph, Inc. announced a $109 million Series A financing to advance a proprietary targeted protein degradation platform and specific programs. Deerfield Management Company established Neomorph earlier this year with scientific founders Phil Chamberlain, DPhil, Eric Fischer, PhD, Benjamin Ebert, MD, PhD, and Scott Armstrong, MD, PhD. /p>                p>The founding management team comprises pharmaceutical veterans with deep industry knowledge in targeted protein degradation drug discovery. Led by Dr. Chamberlain as President and Chief Scientific Officer, Neomorph has recruited top industry talent who have made major contributions to the field, including: Rohan Beckwith, PhD; Gang Lu, PhD; Mary Matyskiela, PhD; Ben Wen, PhD, and Samer Chmait. /p>                p>Targeted protein degradation offers opportunities to develop novel therapeutics across a broad range of disease areas, including oncology. Strategies for protein degradation have been shown to solve critical problems in drug discovery by enabling researchers to target previously ‘undruggable’ proteins that lack suitable binding pockets required for conventional drug activity. /p>                p>Of particular note, Neomorph’s founders are responsible for several fundamental scientific developments in the “molecular glue” field. Molecular glues are types of molecules that encourage proteins to come together that normally wouldnt interact. Neomorph plans to build on the collective pivotal research findings of the team to advance the technology of targeted protein degradation and solve critical problems in human health./p>                p>“Having the ability to achieve this milestone during these unprecedented times is a testament to Neomorph’s capabilities in the protein degradation and molecular glue space,” said Dr. Fischer, who is also an Associate Professor in the Department of Biological Chemistry and Molecular Pharmacology at Harvard Medical School and an Independent Investigator at the Dana-Farber Cancer Institute. “I am humbled to be a part of a team poised to make real strides in advancing the science. We believe we are in an excellent position to take our technology to the next level with the ultimate goal of delivering transformative treatments to patients in need.”  /p>                p>“The Neomorph team has deep expertise in pharmacological approaches to targeted protein degradation and we are excited to be developing new therapeutics for patients with diseases that are currently difficult to treat,” said Dr. Armstrong, who is also David G. Nathan, MD, Professor of Pediatrics at Harvard Medical School and the Dana-Farber Cancer Institute./p>                p>Utilizing Deerfield seed funding and operational support since the first quarter of 2020, Neomorph has established a research site in San Diego at the Genesis Science Center in Sorrento Mesa, California. This Series A financing will position Neomorph to further develop its platform, advance lead programs, and expand the research team. /p>                p>“As a drug strategy, protein degradation has enormous potential as it leverages the cell’s natural system for clearing unwanted or damaged proteins,” said Deerfield Partner Cameron Wheeler, PhD. “We believe there continues to be a significant opportunity in protein degradation, in particular as it relates to the glue space. Neomorph is in an exceptional position and couldn’t have a more seasoned and knowledgeable team in place to interrogate and advance drug targets. The Company’s success could potentially lead to life-altering therapies.”/p>                p>Neomorph will benefit from a close collaboration with the Center for Protein Degradation at Dana Farber Cancer Institute. With its investment, this expands Deerfield’s commitment in the space given the firm’s longstanding partnership and collaboration with Dana Farber Cancer Institute./p>                br>                h5>About Neomorph, Inc./h5>                p>A venture-backed biotechnology company based in San Diego, California, Neomorph is building a leading protein degradation entity, focused on ‘molecular glue’ degraders. Neomorph’s mission is to use this technology to solve critical problems in human health with the discovery and development of innovative new medicines against ‘undruggable targets’. /p>                p>Neomorph comprises scientific leaders from academia and industry who have demonstrated years of commitment and success in the field, and who remain dedicated to advancing the science and technology and delivering highly impactful drugs. The Neomorph team intends to concentrate their efforts on accelerating molecular glue drug discovery, while shepherding a pipeline of projects through clinical development. The Company maintains an important close affiliation with the Center for Protein Degradation at the Dana Farber Cancer Institute./p>                p>Contacts:br>                    Investor Contact: a hrefmailto:inquiries@neomorph.com>inquiries@neomorph.com/a>br>                    Media Contact: a hrefmailto:media@neomorph.com>media@neomorph.com/a>                /p>            /div>            div classnews-article idarticle2 styledisplay:none;>                h2>a target_blank hrefhttps://www.businesswire.com/news/home/20211129005050/en/Philip-Chamberlain-Named-as-Chief-Executive-Officer-of-Neomorph>                    Philip Chamberlain Named as Chief Executive Officer of Neomorph                /a>/h2>                p>SAN DIEGO, November 29th, 2021--(BUSINESS WIRE)--Neomorph, Inc., a venture backed biotechnology company solving critical problems in human health through the discovery and development of innovative new medicines against ‘undruggable targets’, announced today that its board of directors has appointed Philip Chamberlain, D.Phil. as Chief Executive Officer./p>                p stylefont-style:italic>“Phil has an outstanding career in biotechnology and his scientific expertise and leadership make him ideally qualified to lead the company through its next chapter. I am delighted to continue working closely with Phil in pushing the boundaries of this exciting therapeutic area.”/p>                p>Chamberlain has extensive biotechnology leadership experience and most recently served as Executive Director at Celgene where he built and led its structural and chemical biology department. Chamberlain was responsible for several fundamental scientific breakthroughs on the mechanism of action of thalidomide analogs as prototype molecular glues, including the structural basis for cereblon binding and neosubstrate recruitment, the definition of the neosubstrate structural degron, and a molecular explanation for the thalidomide teratogenicity tragedy. Based on these discoveries, he led the construction of the cereblon modulator platform at Celgene, the pioneering drug discovery effort in the molecular glue field. Chamberlain has published work on targeted protein degradation in journals including Nature, Nature Structural and Molecular Biology and Nature Chemical Biology./p>                p>“Phil was integral to the founding of Neomorph and is passionate about pushing the boundaries of new modalities to enable the discovery of advanced new therapeutics,” said Cam Wheeler, Ph.D., Deerfield Management Partner. “We are excited to welcome him as Chief Executive Officer and look forward to benefiting from his expertise and leadership as Neomorph continues its growth strategy.”/p>                p>“I am honored to take on the role of CEO as we advance on our mission to discover transformational therapeutics,” said Chamberlain. “I have been working in the degrader field for more than a decade, and co-founding Neomorph has provided an opportunity to build a specialist molecular glue company from the ground up. We have assembled a wonderful team of employees, founders, and investors, all of whom share the deepest commitment to the field. I am extremely excited to see what we will be able to achieve.”/p>                p>“Neomorph will be well served under Phil’s capable leadership,” said Eric Fischer, co-founder of Neomorph and Independent Investigator at the Dana-Farber Cancer Institute. “Phil has an outstanding career in biotechnology and his scientific expertise and leadership make him ideally qualified to lead the company through its next chapter. I am delighted to continue working closely with Phil in pushing the boundaries of this exciting therapeutic area.”/p>                h5>About Neomorph/h5>                p>Neomorph is a venture backed biotechnology company solving critical problems in human health through the discovery and development of innovative new medicines against undruggable targets./p>                p>Neomorph’s team is comprised of industry leading experts in protein degradation and molecular glues who have a track record of ground-breaking discoveries in the field. The team at Neomorph is committed to leadership in advancing the science and technology of molecular glue drug discovery, while prosecuting a pipeline of projects through clinical development./p>                p>Neomorph is headquartered in San Diego, California./p>                p>Contacts:br>                    Investor Contact: a hrefmailto:inquiries@neomorph.com>inquiries@neomorph.com/a>br>                    Media Contact: a hrefmailto:media@neomorph.com>media@neomorph.com/a>                /p>            /div>            div classnews-article idarticle3 styledisplay:none;>                a target_blank hrefhttps://www.businesswire.com/news/home/20220310005229/en/Neomorph-Inc.-to-Participate-in-Upcoming-Guggenheim-Healthcare-Talks-%E2%80%93-Targeted-Protein-Degradation-Day>                    h2>Neomorph, Inc. to Participate in Upcoming Guggenheim Healthcare Talks – Targeted Protein Degradation Day/h2>                /a>                p classarticle-date>                    March 10, 2022 08:00 AM Eastern Standard Time                /p>                p>                    SAN DIEGO--(a target_blank hrefhttps://www.businesswire.com/>BUSINESS WIRE/a>)--Neomorph, Inc., a rapidly growing biotechnology company comprised of industry leading experts in the field of targeted protein degradation (TPD), today announced that it will participate in an upcoming virtual investor conference:                /p>                p>                    strong>Guggenheim Healthcare Talks - Targeted Protein Degradation Day:/strong> Fireside chat led by Phil Chamberlain, D.Phil., Co-Founder, President, & Chief Executive Officer on Wednesday, March 16, 2022, at 3:30pm ET.                /p>                p>                    Presentation webcasts will be available in the News section of Neomorph’s website                    a hrefhttps://neomorph.com/index.html#news>https://neomorph.com/index.html#news/a>.                /p>                p>strong>About Neomorph/strong>/p>                p>                    Neomorph is a venture backed biotechnology company solving critical problems in human health by discovering innovative new medicines against ‘undruggable’ targets. Our team is comprised of industry leading experts in protein degradation and molecular glues who have a track record of ground-breaking discoveries in the field. We are committed to leadership in advancing the science and technology of molecular glue drug discovery, while prosecuting a pipeline of projects through clinical development. Our patient-first, science-driven approach is complemented by our dedication to a supportive and collaborative work environment. Neomorph is headquartered in San Diego, California.                /p>                h5>Contacts:/h5>                p>                    Investor Contact: a hrefmailto:inquiries@neomorph.com>inquiries@neomorph.com/a>br>                    Media Contact: a hrefmailto:media@neomorph.com>media@neomorph.com/a>                /p>            /div>            div classnews-article idarticle4 styledisplay:none;>                h2>Guggenheim Healthcare Talks - Targeted Protein Degradation Day/h2>                p>                    March 16, 2022, at 3:30pm ET                    br>br>                    Fireside chat led by Phil Chamberlain, D.Phil., Co-Founder, President, & Chief Executive Officer on Wednesday,                    March 16, 2022, at 3:30pm ET                    br>br>                    a classnews-click-here hrefhttps://kvgo.com/guggenheim/neomorph-march-2022 target_blank>Click here for Webcast/a>                /p>            /div>            div classnews-article idarticle5 styledisplay:none;>                h2>Neomorph Announces Multi-Target Collaboration with Novo Nordisk to Discover Novel Molecular Glue Degraders for Cardiometabolic and Rare Diseases/h2>                ul>                    li>Collaboration leverages Neomorph’s leading molecular glue discovery platform and Novo Nordisk’s extensive expertise in cardiometabolic and rare diseases/li>                    li>Total potential deal value of $1.46B across multiple targets/li>                /ul>                p>                    SAN DIEGO, Feb. 26, 2024 /PRNewswire/ -- a hrefhttps://neomorph.com/index.html#home>Neomorph, Inc./a> today announced it has entered into a collaboration and licensing agreement with global healthcare company Novo Nordisk to discover, develop and commercialize molecular glue degraders. Neomorph, a biotechnology company solving critical problems in human health through the discovery of novel therapeutics against ‘undruggable’ targets, was founded in 2020 and is venture backed by Deerfield Management Company.                /p>                p>                    “We are incredibly excited to partner with Novo Nordisk, a world-class healthcare company within diabetes, obesity and rare blood disorders,” said Phil Chamberlain, DPhil, Co-Founder, President, and CEO of Neomorph. “By combining Neomorph’s proprietary glue discovery platform with Novo Nordisk’s vast experience in cardiometabolic and rare diseases, we are well positioned to develop transformative treatments in these areas. This collaboration will enable the expansion of our platform into new therapeutic areas, complementing our on-going efforts in oncology.”                /p>                p>                    Under the terms of the agreement, Neomorph will receive an upfront and near-term milestone payments, plus R&D funding. Neomorph is also eligible to receive future clinical, commercial and sales milestone payments bringing the total potential deal value for multiple targets to $1.46B, plus tiered royalties. Neomorph will lead discovery and preclinical activities against selected targets with Novo Nordisk having the right to exclusively pursue further clinical development and commercialization of the compounds.                /p>                p>                    Novo Nordisk is expanding its drug discovery efforts and deploying a range of novel technology platforms with the aim of discovering and developing new treatment solutions for people living with serious chronic diseases. We are pleased to enter this research collaboration and eager to start the scientific work on the novel class of molecular glue degraders being pioneered by Neomorph,” said Brian Vandahl, Senior Vice President of Global Research Technologies at Novo Nordisk.                /p>                p>strong>About Neomorph/strong>/p>                p>                    Neomorph is a biotechnology company solving critical problems in human health through the discovery and development of innovative new medicines against ‘undruggable’ targets. Neomorph was founded in 2020 and is venture backed by Deerfield Management Company.                /p>                p>                    Neomorph’s team is comprised of industry leading experts in protein degradation and molecular glues who have a track record of ground-breaking discoveries in the field. The team at Neomorph is committed to leadership in advancing the science and technology of molecular glue drug discovery, while prosecuting a pipeline of projects through clinical development.                /p>                p>                    Neomorph is headquartered in San Diego, California. For more information, visit a hrefhttp://www.neomorph.com/>www.neomorph.com/a> and follow us on a hrefhttps://www.linkedin.com/company/neomorph-llc/mycompany/>LinkedIn/a>.                /p>                h5>Contacts:/h5>                p>                    Investor Contact: a hrefmailto:inquiries@neomorph.com>inquiries@neomorph.com/a>br>                    Media Contact: a hrefmailto:media@neomorph.com>media@neomorph.com/a>                /p>            /div>            div classnews-article idarticle6 styledisplay:none;>                h2>Biogen and Neomorph Announce Multi-Target Research Collaboration                     to Discover and Develop Molecular Glue Degraders for Alzheimers, Rare, and Immunological Diseases                /h2>                ul>                    li>The collaboration aims to discover and develop molecular glue degrader clinical candidates for priority targets to Biogen/li>                    li>Collaboration leverages Neomorphs leading molecular glue discovery platform and Biogens deep expertise in Alzheimers, rare, and immunological diseases./li>                /ul>                p>                    strong>Cambridge, Mass. and San Diego, Calif., - October 29, 2024/strong> - a hrefhttp://www.biogen.com/>Biogen Inc./a> (Nasdaq: BIIB) and Neomorph Inc. announced a research                     collaboration to discover and develop molecular glue degraders for priority targets in Alzheimers, rare neurological, and immunological diseases                /p>                p>                As part of the collaboration, the companies aim to utilize Neomorphs proprietary molecular glue discovery platform to accelerate the identification and validation of novel small molecule therapeutic molecular glue degraders. Small molecule protein degraders have been shown to effectively drug challenging targets with differentiated pharmacology from more traditional inhibitors. Pursuing innovative solutions aimed at modulating protein levels through targeted degradation holds promise for treating complex neurological, immunological and rare diseases. This collaboration will leverage Neomorph’s research strengths in targeted protein degradation and Biogen’s deep scientific expertise and drug development capabilities.                /p>                p>                As part of our modality agnostic research strategy, Biogen is committed to investing in new approaches to unlock biological targets that have remained difficult to reach, said Jane Grogan, Ph.D., Head of Research at Biogen. This collaboration with Neomorph reflects the approach we want to take to pair our internal drug development expertise with cutting-edge external innovation to create clinically meaningful therapies for patients.                /p>                p>                Neomorphs molecular glue degrader platform represents a unique approach to drug discovery, said Phil Chamberlain, DPhil, Co-Founder, President, and Chief Executive Officer of Neomorph. We are excited to partner with Biogen, a leader in Alzheimers, rare, and immunological diseases, to explore the potential of our technology in addressing some of the most challenging and valuable targets in these fields.                /p>                p>                Under the terms of the agreement, Biogen and Neomorph will collaborate to identify, validate, and optimize small molecule molecular glue degraders for several high-priority targets and Biogen will advance clinical candidates for further development and potential commercialization. Neomorph will receive an upfront payment and is eligible to receive contingent milestone payments per target as the collaboration progresses through various stages. These include certain pre-clinical milestones payable in the near-term and certain clinical, regulatory, commercial and sales milestones that are anticipated to occur later this decade and beyond, for a total consideration of up to $1.45B. Biogen will reimburse Neomorph for certain research development costs. Neomorph is also eligible to receive potential future royalties in the mid-single digit to low double-digit range                /p>                p>                strong>About Biogen/strong>br>                Founded in 1978, Biogen is a leading biotechnology company that pioneers innovative science to deliver new medicines to transform                 patients lives and to create value for shareholders and our communities. We apply deep understanding of human biology and leverage                 different modalities to advance first-in-class treatments or therapies that deliver superior outcomes. Our approach is to take bold risks,                 balanced with return on investment to deliver long-term growth.                /p>                p>                We routinely post information that may be important to investors on our website at a hrefhttps://www.biogen.com/>www.biogen.com/a>.                 Follow us on social media - a hrefhttps://www.facebook.com/Biogen/>Facebook/a>, a hrefhttps://www.linkedin.com/company/biogen-/>LinkedIn/a>,                     a hrefhttps://twitter.com/biogen>X/a>, a hrefhttps://www.youtube.com/c/biogen>YouTube/a>.                /p>                p>                strong>About Neomorph/strong>br>                Neomorph is a biotechnology company solving critical problems in human health through the discovery and development of innovative new medicines                 against undruggable targets. Neomorph was founded in 2020 and is venture-backed by Deerfield Management Company.br>                Neomorphs team is comprised of industry-leading experts in protein degradation and molecular glues who have a track record of groundbreaking                 discoveries in the field. The team at Neomorph is committed to leadership in advancing the science and technology of molecular glue drug                 discovery while prosecuting a pipeline of projects through clinical development.br>                Neomorph is headquartered in San Diego, California. For more information, visit a hrefhttp://www.neomorph.com/>www.neomorph.com/a>                     and follow us on a hrefhttps://www.linkedin.com/company/neomorph-llc/mycompany/>LinkedIn/a>.                /p>                p>                strong>Biogen Safe Harbor/strong>br>                This press release contains forward-looking statements, including statements relating to our strategy and plans; potential of, and expectations for, our commercial business and pipeline programs; capital allocation and investment strategy; clinical development programs, clinical trials, and data readouts and presentations; the potential for molecular glue degraders; regulatory discussions, submissions, filings, and approvals; and the potential benefits, safety, and efficacy of our and our collaboration with Neomorph. These forward-looking statements may be accompanied by words such as aim, anticipate, believe, could, estimate, expect, forecast, goal, intend, may, plan, potential, possible, prospect, will, would, and other words and terms of similar meaning. Drug development and commercialization involve a high degree of risk, and only a small number of research and development programs result in commercialization of a product. Results in early-stage clinical trials may not be indicative of full results or results from later-stage or larger-scale clinical trials and do not ensure regulatory approval. You should not place undue reliance on these statements.                /p>                p>                These statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements, including our dependence on sales from our products; uncertainty of long-term success in developing, licensing, or acquiring other product candidates or additional indications for existing products; failure to compete effectively; failure to successfully execute or realize the anticipated benefits of our strategic and growth initiatives; difficulties in obtaining and maintaining adequate coverage, pricing, and reimbursement for our products; our dependence on collaborators and other third parties for the development, regulatory approval, and commercialization of products and other aspects of our business, which are outside of our full control; risks associated with current and potential future healthcare reforms; risks related to commercialization of biosimilars; failure to obtain, protect, and enforce our data, intellectual property, and other proprietary rights; and the risks and uncertainties relating to intellectual property claims and challenges.                /p>                p>                These statements speak only as of the date of this press release. We do not undertake any obligation to publicly update any forward-looking statements.                /p>                h5>Contacts:/h5>                p>                    strong>Investor Contact(s)/strong>br>                    Biogen: a hrefmailto:IR@biogen.com >IR@biogen.com /a>br>                    Neomorph: a hrefmailto:inquiries@neomorph.com>inquiries@neomorph.com/a>                    br>br>                    strong>Media Contact(s)/strong>br>                    Biogen: a hrefmailto:public.affairs@biogen.com>public.affairs@biogen.com/a>br>                    Neomorph: a hrefmailto:media@neomorph.com>media@neomorph.com/a>                /p>                    /div>        /div>    /div>/div>style>    separator {        display:block;        padding: .5px 0;        margin: 2rem 0;        border:0;        height:1px;        width: 60%;        background-color: #2a397288;    }/style>        !-- Leadership page -->        div classleadership-content screen hidden idleadership>    div classleadership-header>        h1>Leadership/h1>    /div>    div classleadership-sub-nav>        div classsub-nav-list>            div classsub-nav management selected onclicktoggleLeaderTabs(management)>                Management            /div>            div classsub-nav founders onclicktoggleLeaderTabs(founders)>                Founders            /div>            div classsub-nav board onclicktoggleLeaderTabs(board)>                Board            /div>            div classsub-nav investors onclicktoggleLeaderTabs(investors)>                Investors            /div>        /div>    /div>    div classleadership-profiles>        div idmanagement classtabs-wrapper leader-profile-grid justify-content-center styledisplay:none;>!--            div classleaderDownArrow>img srcimages/careers/arrowManageDown.png>/div>-->            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Chamberlain)>                    img src./images/leadership/PhilC_new.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/PhilC_new.png/>                /div>                div classleader-name>                    Philip Chamberlain                /div>                div classleader-bio Chamberlain styledisplay:none;>                    p>                        Phil is Co-Founder, President, and CEO of Neomorph. He obtained his BA and D.Phil. degrees from the University of Oxford before traveling to the U.S. to work at the Genomics Institute of the Novartis Research Foundation (GNF). At GNF Phil supported and led projects in serious respiratory and inflammatory disease and solved multiple novel structures. Phil joined Celgene, San Diego in 2007 and built and led the Structural and Chemical Biology department, most recently as Executive Director, Protein Homeostasis and Structural Biology. Phil was responsible for several fundamental scientific breakthroughs on the mechanism of action of thalidomide analogs, including the structural basis for cereblon binding and neosubstrate recruitment, the definition of the neosubstrate ‘structural degron’, and a plausible molecular explanation for the thalidomide teratogenicity disaster of the twentieth century. Based on these discoveries, Phil led the construction of the cereblon modulator platform at Celgene, the pioneering drug discovery effort in the ‘molecular glue’ field generating a portfolio of projects. Phil has published work on targeted protein degradation in journals including Nature, Nature Structural and Molecular Biology and Nature Chemical Biology. Phil was the recipient of the John W. Jackson leadership award, the most prestigious achievement award at Celgene.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Klaus)>                    img  srcimages/leadership/klaus-wagner.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/klaus-wagner.png/>                /div>                div classleader-name>                    Klaus Wagner                /div>                div classleader-bio Klaus styledisplay:none;>                    p>                        Dr. Wagner has over 20 years of experience in cancer research and clinical drug development, most recently as Chief Medical Officer at Boundless Bio, Inc., where he guided the clinical development of the companys pipeline of novel small molecule therapeutics targeting patients with oncogene amplifications.                         Prior to that, Dr. Wagner built and led an integrated clinical development organization at Inhibrx, Inc., where he was responsible for advancing four single-domain antibody-based and Fc fusion protein therapeutic candidates from pre-IND into the clinic, including three oncology programs.                         Dr. Wagner trained and completed his fellowship in Medical Oncology at MD Anderson Cancer Center. As a board-certified Medical Oncologist, who continues to treat cancer patients, he practiced at Banner MD Anderson Cancer Center and served as Adjunct Assistant Professor in the Department of Thoracic, Head & Neck Medical Oncology at MD Anderson Cancer Center, where he led molecularly targeted therapy and cancer immunotherapy trials in non-small cell lung cancer as a local principal investigator.                         His scientific work at Genentech, Inc. and the Genomics Institute of the Novartis Research Foundation focused on molecularly targeted cancer drug discovery and predictive biomarker development. Dr. Wagner received his M.D. and Ph.D. from the Friedrich-Alexander University of Erlangen in Germany and was a scholar of the German National Academic Scholarship Foundation.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Beckwith)>                    img src./images/leadership/Rohan_new.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/Rohan_new.png/>                /div>                div classleader-name>                    Rohan  Beckwith                /div>                div classleader-bio Beckwith styledisplay:none;>                    p>                        Rohan Beckwith, Ph.D. is Sr. Vice President of Chemistry at Neomorph bringing over 15 years of experience in Drug Discovery, 7 in the field of targeted protein degradation.  He most recently served as a Director in the Chemical Biology and Therapeutics group at the Novartis Institutes for BioMedical Research, where he was a key contributor in building a molecular glue degrader platform, from which he led efforts to establish drug discovery programs and delivered a clinical candidate.  He has developed molecular glue degraders for CRBN, VHL and DCAF15 E3 ligases.  In addition, Rohan has worked on over 20 research projects across various therapeutic areas, such as HECT E3 ligase inhibitors, modulators of RNA processing, Wnt pathway modulators, IAP, spinal muscular atrophy, synthetic RNA delivery, cytokine receptors, chemokine receptors, kinases).  He has led multi-disciplinary teams in chemical biology and target identification efforts, as well as hit-to-lead and lead optimization.  Prior to joining Novartis, Rohan conducted postdoctoral training with Prof. Huw Davies in the field of rhodium carbenoid-mediated C-H activation.  He received his Ph.D. in synthetic organic chemistry from University of Nottingham, U.K. and before that his MSci. Chem from Bristol University, U.K.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Matyskiela)>                    img src./images/leadership/MaryM_new.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/MaryM_new.png/>                /div>                div classleader-name>                    Mary Matyskiela                /div>                div classleader-bio Matyskiela styledisplay:none;>                    p>                        Mary Matyskiela, Ph.D. is Vice President of Molecular Sciences at Neomorph and brings                        more than 20 years of experience in the ubiquitin-proteasome field. Mary received her                        B.S. in Chemistry from Yale University, where she performed undergraduate research in                        the lab of Dr. Craig Crews. She then moved to the University of California San Francisco                        for graduate work on ubiquitin ligase mechanism in the lab of Dr. David Morgan. She went                        on to perform postdoctoral research at the University of California Berkeley, studying                        the structure and function of the 26S proteasome with Dr. Andreas Martin, HHMI.                        Following her academic training, she moved to Celgene and Bristol Myers Squibb, where                        she spent 6 years working in targeted protein degradation drug discovery, most recently                        as Associate Director of Structural Biology and Proteomics, Oncology West. Mary is known                        for her work in elucidating the molecular mechanisms and expanding the horizons of                        molecular glue targeting through cereblon-CRL4, and is an author of foundational                        publications in the molecular glue field.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Wen)>                    img src./images/leadership/BenWen_new.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/BenWen_new.png/>                /div>                div classleader-name>                    Ben Wen                /div>                div classleader-bio Wen styledisplay:none;>                    p>                        Ben Wen, Ph.D. is Vice President of Biology at Neomorph with over 15 years of experience in drug discovery pharmacology. Prior to Neomorph, Ben was at the Genomics Institute of the Novartis Research Foundation (GNF) where he conducted his postdoc in T cell development and continued on into varying roles of increasing responsibility in the departments of pharmacology and cancer therapeutics. He has experience in progressing projects from inception to clinical investigation in the areas of autoimmunity, inflammation, allergy, cancer, infectious disease, and transplant conditioning. He received his BA in Molecular and Cellular Biology from UC Berkeley and his Ph.D. in Biology with a focus in immunology from UC San Diego.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Grant)>                    img src./images/leadership/Ana_new.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/Ana_new.png/>                /div>                div classleader-name>                    Ana Grant                /div>                div classleader-bio Grant styledisplay:none;>                    p>                        Ana Grant, Ph.D. is Vice President, Data Sciences at Neomorph, with over 20 years of experience in bioinformatics, data science, scientific software support and data workflow automation.  Originally from Portugal, Ana trained first in the U.K., obtaining her B.Sc. in Genetics from the University of Leeds, then M.Res. in Bioinformatics and D.Phil. in Chemistry from the University of York.  It was at the York Structural Biology Laboratory, whilst developing a system for target selection from genomic sequences, that she discovered her passion for collaboration.  As a Postdoctoral Associate at The Salk Institute, Ana worked on numerous collaborations applying data science to derive genome-wide insights on the transcriptional regulation of aging and protein homeostasis.  Following her academic training, she moved to the University of Michigan, where she balanced her time between genomics research and supporting state-of-the-art OMICs analysis needs across the campus, initially for the Bioinformatics Core and later as Bioinformatics Manager for the Epigenomics Core.  Prior to Neomorph, Ana was Director of Research Informatics at Synthetic Genomics, where she led a team of Bioinformaticians, Data Scientists and Software Engineers to develop an informatics platform to support algae biofuel research. There she solidified her track record on protein function and structure annotation, as well as leveraging her expertise to ensure people and systems have the software and analytics they need to do innovative science.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Zhong)>                    img src./images/leadership/Bell_Zhong.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/Bell_Zhong.png/>                /div>                div classleader-name>                    Bell Zhong                /div>                div classleader-bio Zhong styledisplay:none;>                    p>                        Bell Zhong is Chief Financial Officer of Neomorph. He is a seasoned finance professional with over 17 years of finance and investment banking experience, advising on capital markets, mergers & acquisitions and other strategic transaction for a wide array of biotechnology and pharmaceutical companies. Throughout his career, he has helped execute over $35bn in equity and equity linked transactions and more than $100bn in M&A transactions for both private and public companies.                        br>br>                        Most recently, Bell was Managing Director, healthcare investment banking at Raymond James & Associates, Inc. where he led the banking coverage efforts on a number of innovative biotech companies.  Prior to Raymond James, Bell spent over 13 years at J.P. Morgan and was an Executive Director in the healthcare investment banking group, covering the healthcare sector.                        br>br>                        Bell holds a B.S. in Finance and Accounting from New York University Leonard N. Stern School of Business.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Chmait)>                    img src./images/leadership/Samer_new.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/Samer_new.png/>                /div>                div classleader-name>                    Samer Chmait                /div>                div classleader-bio Chmait styledisplay:none;>                    p>                        Samer Chmait is Vice President, Research Operations at Neomorph. Prior to Neomorph, Samer was Head of Scientific Operations at Strateos Inc where he enabled the access of a remote-controlled lab to other drug discovery companies and research scientists through Strateos’ secure cloud-based platform. With over a decade of chemistry training and experience, Samer’s early research focused on the purification, crystallization, and structure elucidation of novel proteins in support of Amgen Inc’s small molecule drug discovery programs. Samer later joined Celgene, San Diego and led the Biology Operations Team to drive both scientific and operational functions forward during company growth and expansion. Samer has over 15 years of biotechnology industry experience and has contributed to 17 publications within prestigious journals.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Gates)>                    img srcimages/leadership/MeganGates_new.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/MeganGates_new.png/>                /div>                div classleader-name>                    Megan Gates                /div>                div classleader-bio Gates styledisplay:none;>                    p>                        Megan Gates is the Vice President of Talent Acquisition at Neomorph, where she leads all aspects of the company’s recruitment strategy, workforce planning, and talent brand development. With over 20 years of experience in Talent Acquisition, Megan has built a career supporting scientific research organizations within the life sciences industry. Prior to joining Neomorph, Megan was the Global Talent Acquisition Lead for Research & Early Development at Bristol Myers Squibb, where she led recruitment strategy and execution for the global R&ED organization following the acquisition of Celgene. Her earlier experience includes talent acquisition leadership and consulting roles at Celgene, Bristol Myers Squibb, Amylin Pharmaceuticals, and Elan Pharmaceuticals.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Marla)>                    img  srcimages/leadership/Marla_new.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/Marla_new.png/>                /div>                div classleader-name>                    Marla Bornstein                /div>                div classleader-bio Marla styledisplay:none;>                    p>                        Marla Bornstein is Sr. Vice President, Business Development for Neomorph. She brings over 20 years of biotech experience in business development, corporate strategy, new product planning, marketing, and regulatory affairs. Most recently, Marla was Senior Director, Business Development at Illumina where she led pharmaceutical companion diagnostic partnerships and established an IVD partnering program for Illumina’s sequencing platforms. At Biogen Idec, Marla played an integral role in portfolio prioritization initiatives and was instrumental in driving oncology new product marketing launch plans. Prior to Biogen Idec, Marla worked as a strategy consultant for Analytica International, performing market assessments and building global pricing and reimbursement strategies for life science companies. Marla began her career in regulatory affairs at Pharmascience. Marla has a BSc in Microbiology and Immunology from McGill University and an MBA from Columbia University.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(SaraWeymer)>                    img srcimages/leadership/sara-weymer.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/sara-weymer.png/>                /div>                div classleader-name>                    Sara Weymer                /div>                div classleader-bio SaraWeymer styledisplay:none;>                    p>                        Sara Weymer is Vice President, Clinical Operations, at Neomorph. She brings over 20 years of clinical development experience focusing on Phase I-III studies in oncology and neurology. She joins Neomorph from Boundless Bio, where she held the position of Vice President, Clinical Operations, and participated in the IND filing and clinical trial start-up of their two lead clinical development programs. While at Boundless, Sara had the opportunity to work on the first studies targeting extrachromosomal DNA in pan-tumor indications using precision medicine. Prior to that, Sara was at Fate Therapeutics, Inc. where she served as Executive Director and Head of Clinical Operations and oversaw the clinical implementation of 9 Fate-sponsored INDs and 6 Investigator-initiated INDs across 8 development programs. During this time Sara had the opportunity to pioneer the clinical development of IPSC-derived NK and T-cell therapies in various hematologic and solid tumor indications. Sara’s early career included positions of increasing responsibility with experience in all types of development organizations including ZZ Biotech, Biogen Idec, Metabasis Therapeutics, Altana Pharma, and Parexel. Sara holds a Bachelor of Science in nutritional biochemistry from Cornell University.                    /p>                /div>            /div>        /div>        div idfounders classtabs-wrapper leader-profile-grid justify-content-center styledisplay:none;>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Chamberlain)>                    img src./images/leadership/PhilC_new.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/PhilC_new.png/>                /div>                div classleader-name>                    Philip Chamberlain                /div>                div classleader-bio Chamberlain styledisplay:none;>                    p>                        Phil is Co-Founder, President, and CEO of Neomorph. He obtained his BA and D.Phil. degrees from the University of Oxford before traveling to the U.S. to work at the Genomics Institute of the Novartis Research Foundation (GNF). At GNF Phil supported and led projects in serious respiratory and inflammatory disease and solved multiple novel structures. Phil joined Celgene, San Diego in 2007 and built and led the Structural and Chemical Biology department, most recently as Executive Director, Protein Homeostasis and Structural Biology. Phil was responsible for several fundamental scientific breakthroughs on the mechanism of action of thalidomide analogs, including the structural basis for cereblon binding and neosubstrate recruitment, the definition of the neosubstrate ‘structural degron’, and a plausible molecular explanation for the thalidomide teratogenicity disaster of the twentieth century. Based on these discoveries, Phil led the construction of the cereblon modulator platform at Celgene, the pioneering drug discovery effort in the ‘molecular glue’ field generating a portfolio of projects. Phil has published work on targeted protein degradation in journals including Nature, Nature Structural and Molecular Biology and Nature Chemical Biology. Phil was the recipient of the John W. Jackson leadership award, the most prestigious achievement award at Celgene.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Fischer)>                    img src./images/leadership/Profile-EricFischer.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/Profile-EricFischer.png/>                /div>                div classleader-name>                    Eric Fischer                /div>                div classleader-bio Fischer styledisplay:none;>                    p>                        Eric Fischer, PhD, is Independent Investigator at Dana-Farber Cancer Institute and Associate Professor of Biological Chemistry and Molecular Pharmacology at Harvard Medical School. He is Co-Director of the Center for Protein Degradation at Dana-Farber Cancer Institute.                        br/>br/>                        Dr. Fischer’s research focuses on understanding the molecular architecture, function, and regulation of complex cellular signaling machines and their involvement in cellular processes, as well as leveraging this knowledge to develop new strategies for small-molecule-mediated modulation. Using biochemistry, chemical biology, and cell biology methods, his lab has contributed to the understanding of the efficacy and adverse activity of thalidomide and analogs. Beyond defining the mechanism of action for this transformative cancer drug and solving a decade-old mystery of pharmaceutical sciences, this work inspired numerous projects that intend to utilize similar principles to redirect ligase activity to new targets. This represents a new therapeutic modality often referred to as targeted protein degradation. Dr. Fischer’s lab helped to establish this approach and has defined many of the underlying principles for small molecules degraders. Dr. Fischer’s work has been recognized with awards including, the Damon Runyon Cancer Research Foundation’s 2017 Damon Runyon-Rachleff Innovation Award, and the Mark Foundation’s 2018 Emerging Leaders Award.                        br/>br/>                        Dr. Fischer completed his undergraduate training at the Universities of Hamburg (Germany) and Basel (Switzerland) and completed doctoral training at the Friedrich Miescher Institute for Biomedical Research, also in Basel. Dr. Fischer joined the Dana-Farber faculty in 2015.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Ebert)>                    img src./images/leadership/Profile-BenjaminEbert.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/Profile-BenjaminEbert.png/>                /div>                div classleader-name>                    Benjamin Ebert                /div>                div classleader-bio Ebert styledisplay:none;>                    p>                        Benjamin L. Ebert, MD, PhD, is president and CEO of Dana-Farber Cancer Institute, Director of Dana-Farber/Harvard Cancer Center and the Richard and Susan Smith Professor of Medicine at Harvard Medical School.                         br/>br/>                        Dr. Ebert is an elected member of the National Academy of Medicine, the American Academy of Arts and Sciences, the American Society for Clinical Investigation, the Association of American Physicians, and the Academy of the American Association for Cancer Research. He served as president of the American Society for Clinical Investigation in 2017. He currently serves on the Board of Directors for the Broad Institute and Break Through Cancer.                         br/>br/>                        The Ebert laboratory focuses on the molecular basis and treatment of hematologic malignancies and its non-malignant precursor conditions, with a particular focus on myelodysplastic syndromes (MDS) and clonal hematopoiesis. The Ebert laboratory demonstrated that lenalidomide, a derivative of thalidomide, binds the CRL4-CRBN E3 ubiquitin ligase and induces degradation of specific substrates. Subsequent research has examined novel mechanisms of drug-induced protein degradation that expand the spectrum of protein substrates that can be targeted pharmacologically.                        br/>br/>                        Dr. Ebert received the William Dameshek Prize from the American Society of Hematology, the Meyenburg Prize for Cancer Research, the Sjöberg Prize from the Royal Swedish Academy of Sciences, and the Korsmeyer Award from the American Society for Clinical Investigation. He has received awards from Harvard Medical School and the Harvard-MIT Health Sciences and Technology Program for mentorship.                        br/>br/>                        Dr. Ebert received a bachelors degree from Williams College and a doctorate from Oxford University as a Rhodes Scholar in the laboratory of Sir Peter Ratcliffe. He completed an M.D. from Harvard Medical School, a residency in internal medicine at Massachusetts General Hospital, and a fellowship in hematology/oncology at the Dana-Farber Cancer Institute.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Armstrong)>                    img src./images/leadership/Profile-ScottArmstrong.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/Profile-ScottArmstrong.png/>                /div>                div classleader-name>                    Scott Armstrong                /div>                div classleader-bio Armstrong styledisplay:none;>                    p>                        Dr. Scott Armstrong is the David G. Nathan Professor of Pediatrics at Harvard Medical School, Chair of Pediatric Oncology at the Dana-Farber Cancer Institute and President of the Dana-Farber/Boston Children’s Cancer and Blood Disorders Center.                        br/>br/>                        The Armstrong laboratory is interested in the relationship between leukemia and normal hematopoietic stem cells, and the mechanisms by which chromatin modifications control gene expression during normal and cancer development. The laboratory has defined developmental gene expression programs that are aberrantly expressed in cancer and identified the chromatin regulatory complexes that are critical for maintenance of cancer-causing gene expression. This work prompted development of small molecules that target chromatin-based mechanisms, a number of which are currently being assessed in adults and children with cancer.                        br/>br/>                        Dr. Armstrong is a member of the National Academy of Medicine and his work has been recognized multiple awards including the Till and McCulloch Award from the International Society of Experimental Hematology, the Wilson S. Stone Award from MD Anderson Cancer Center, the Paul Marks Prize for Cancer Research from Memorial Sloan Kettering Cancer Center, the E. Mead Johnson Award from the Society for Pediatric Research and the Dameshek Prize from the American Society of Hematology.                        br/>br/>                        Dr. Armstrong received his MD and PhD from the University of Texas Southwestern Medical School in Dallas, Texas where he performed his PhD under the mentorship of Nobel laureates Michael Brown and Joseph Goldstein. He performed his residency and fellowship in pediatric hematology/oncology at Children’s Hospital Boston, the Dana Farber Cancer Institute, and Harvard Medical School.                    /p>                /div>            /div>        /div>        div idboard classtabs-wrapper leader-profile-grid justify-content-center styledisplay:none;>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Chamberlain)>                    img src./images/leadership/PhilC_new.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/PhilC_new.png/>                /div>                div classleader-name>                    Philip Chamberlain                /div>                div classleader-bio Chamberlain styledisplay:none;>                    p>                        Phil is Co-Founder, President, and CEO of Neomorph. He obtained his BA and D.Phil. degrees from the University of Oxford before traveling to the U.S. to work at the Genomics Institute of the Novartis Research Foundation (GNF). At GNF Phil supported and led projects in serious respiratory and inflammatory disease and solved multiple novel structures. Phil joined Celgene, San Diego in 2007 and built and led the Structural and Chemical Biology department, most recently as Executive Director, Protein Homeostasis and Structural Biology. Phil was responsible for several fundamental scientific breakthroughs on the mechanism of action of thalidomide analogs, including the structural basis for cereblon binding and neosubstrate recruitment, the definition of the neosubstrate ‘structural degron’, and a plausible molecular explanation for the thalidomide teratogenicity disaster of the twentieth century. Based on these discoveries, Phil led the construction of the cereblon modulator platform at Celgene, the pioneering drug discovery effort in the ‘molecular glue’ field generating a portfolio of projects. Phil has published work on targeted protein degradation in journals including Nature, Nature Structural and Molecular Biology and Nature Chemical Biology. Phil was the recipient of the John W. Jackson leadership award, the most prestigious achievement award at Celgene.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Lebowitz)>                    img src./images/leadership/peter-lebowitz.png />                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/peter-lebowitz.png />                /div>                div classleader-name>                    Peter Lebowitz                /div>                div classleader-bio Lebowitz styledisplay:none;>                    p>                        Peter Lebowitz currently serves as the CEO of Third Arc Bio. Prior to Third Arc, he was the Global Head of Oncology R&D                        for Johnson & Johnson, where he built a world-class, end-to-end J&J oncology team that delivered 13 new oncology drugs                        by leveraging both internal R&D excellence and external partnerships. Peter also held senior leadership positions in                        discovery and early/late-stage clinical development at GlaxoSmithKlein. Throughout his tenure in the pharmaceutical                        industry, he achieved 15 major product approvals and successfully filed over 40 Investigational New Drug applications.                        Peter also served as Assistant Professor of Medicine, Division of Hematology/Oncology at the Lombardi Comprehensive                        Cancer Center at Georgetown University Medical Center, where he established a translational and clinical research                        program as a practicing oncologist. Peter graduated magna cum laude from Harvard University and received his M.D. and                        Ph.D. from the University of Pennsylvania School of Medicine. He completed his postgraduate clinical training in                        Internal Medicine at Duke University Medical Center and his Hematology/Oncology fellowship at the National Cancer                        Institute, National Institute of Health.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Wheeler)>                    img src./images/leadership/Profile-CameronWheeler.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/Profile-CameronWheeler.png/>                /div>                div classleader-name>                    Cameron Wheeler                /div>                div classleader-bio Wheeler styledisplay:none;>                    p>                        Cameron Wheeler, Ph.D., is a Partner on the Biotherapeutics group at Deerfield and joined the Firm in 2014. Prior to Deerfield, Dr. Wheeler worked for and on behalf of Eleven Biotherapeutics, Inc. as a director since 2009. Previous to that, he was Manager of the Business Development and Operations team at Constellation Pharmaceuticals, Inc. and a Senior Associate at Third Rock Ventures, LLC. Dr. Wheeler holds a Ph.D. and S.M. in Biological Engineering and an S.B. in Mechanical Engineering from the Massachusetts Institute of Technology                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Fischer)>                    img src./images/leadership/Profile-EricFischer.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/Profile-EricFischer.png/>                /div>                div classleader-name>                    Eric Fischer                /div>                div classleader-bio Fischer styledisplay:none;>                    p>                        Eric Fischer, PhD, is Independent Investigator at Dana-Farber Cancer Institute and Associate Professor of Biological Chemistry and Molecular Pharmacology at Harvard Medical School. He is Co-Director of the Center for Protein Degradation at Dana-Farber Cancer Institute.                        br/>br/>                        Dr. Fischer’s research focuses on understanding the molecular architecture, function, and regulation of complex cellular signaling machines and their involvement in cellular processes, as well as leveraging this knowledge to develop new strategies for small-molecule-mediated modulation. Using biochemistry, chemical biology, and cell biology methods, his lab has contributed to the understanding of the efficacy and adverse activity of thalidomide and analogs. Beyond defining the mechanism of action for this transformative cancer drug and solving a decade-old mystery of pharmaceutical sciences, this work inspired numerous projects that intend to utilize similar principles to redirect ligase activity to new targets. This represents a new therapeutic modality often referred to as targeted protein degradation. Dr. Fischer’s lab helped to establish this approach and has defined many of the underlying principles for small molecules degraders. Dr. Fischer’s work has been recognized with awards including, the Damon Runyon Cancer Research Foundation’s 2017 Damon Runyon-Rachleff Innovation Award, and the Mark Foundation’s 2018 Emerging Leaders Award.                        br/>br/>                        Dr. Fischer completed his undergraduate training at the Universities of Hamburg (Germany) and Basel (Switzerland) and completed doctoral training at the Friedrich Miescher Institute for Biomedical Research, also in Basel. Dr. Fischer joined the Dana-Farber faculty in 2015.                    /p>                /div>            /div>            div classleader-profile>                div classleader-profile-photo onclickshowLeaderBio(Pearlberg)>                    img src./images/leadership/Profile-JoePearlberg.png/>                /div>                div classleader-profile-photo-square styledisplay:none;>                    img src./images/leadership/Profile-JoePearlberg.png/>                /div>                div classleader-name>                    Joseph Pearlberg                /div>                div classleader-bio Pearlberg styledisplay:none;>                    p>                        Joseph Pearlberg, M.D., Ph.D., is the Vice President of Scientific Affairs on the Biotherapeutics group at Deerfield and joined the Firm in 2017. Prior to Deerfield, Dr. Pearlberg was the Vice President of Clinical Development at Infinity Pharmaceuticals. Before Infinity Pharmaceuticals, Dr. Pearlberg worked as a Medical Director in the oncology unit of Sanofi. Dr. Pearlberg received his M.D. at the University of California, San Francisco, and completed his clinical training at the Massachusetts General Hospital and Dana Farber Cancer Institute. He earned his Ph.D. in Molecular Biology from Harvard University and was a Lecturer in the Department of Biological Chemistry and Molecular Pharmacology at Harvard Medical School. He holds a B.A. in Biochemistry from the University of Pennsylvania.                    /p>                /div>            /div>        /div>        div idinvestors classtabs-wrapper row justify-content-center styledisplay:none;>            div classleader-profile col-12 stylepadding-left:10vw;>                div classleader-profile-photo deerfield-photo-logo>                    img src./images/leadership/Deerfield%20logo-01.png/>                /div>                div classleader-name>                    Deerfield is an investment management firm committed to advancing healthcare through investment, br/>                    information and philanthropy.                /div>            /div>        /div>    /div>    div classleadership-profile-view>        div classleadership-back-button onclickleadershipBackClick()>/div>        div classleader>            div classleader-profile-photo-view>            /div>            div classleader-name-view>            /div>        /div>        div classleader-bio-view>        /div>    /div>/div>        !-- Careers page -->        div classcareers-content screen hidden idcareers>    div classcareers-header>        h1>Join Our Team/h1>    /div>    div classcareers-paragraph idcareerSection>        !--                div classcareers-button onclickcareerScrollDown()>-->        a hrefcareers.html styletext-decoration:none;>            div classcareers-button>                View Job Opportunities            /div>        /a>        div classcareers-chart>            div classcareers-chart-title>                Our Core Values            /div>            div classcareers-chart-svg>                svg xmlnshttp://www.w3.org/2000/svg                     viewBox0 0 893.25 924.43                     styleenable-background:new 0 0 893.25 924.43;overflow:visible>                    defs>                        style>                            .cls-1,.cls-8,.cls-9{fill:none;stroke-linecap:round;}                            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dM687.11,523.62v1.86H687a4.08,4.08,0,0,0-3-1c-1.24,0-2,.58-2,1.44,0,.7.51,1,2.12,1.12,2.64.14,3.61,1,3.61,2.92s-1.46,3-3.81,3a5.76,5.76,0,0,1-3.67-1V530h.08a4.52,4.52,0,0,0,3.53,1.34c1.31,0,2.14-.56,2.14-1.45s-.54-1.15-2.27-1.26c-2.53-.16-3.46-1-3.46-2.72s1.48-3.07,3.73-3.07A6,6,0,0,1,687.11,523.62Z transformtranslate(-106.27 -18.15)/>path classcls-5 dM692.06,531.75a1.15,1.15,0,0,1-1.17,1.19,1.2,1.2,0,1,1,0-2.39A1.15,1.15,0,0,1,692.06,531.75Z transformtranslate(-106.27 -18.15)/>                    /g>                /svg>            /div>        /div>        div classcareers-cards>            div classcareers-card>                div classcareers-card-title>                    Benefits                /div>                div classcareers-card-body>                    img srcimages/careers/downarrow.png altcard down arrow onclickRevealCard(cardOne)>                    div classcareers-card-body-paragraph idcardOne>                        img srcimages/careers/uparrow.png altcard up arrow onclickHideCard(cardOne)>                        br>br>                        We offer a robust benefits package to ensure our employees stay healthy. This includes a comprehensive choice of HMO, PPO and High Deductible medical plans, including a Health Savings Account with employer funding. We realize the importance of tax deferred savings options and provide Flexible Spending Accounts for health and dependent care reimbursements.  We also provide 100% company sponsored dental and vision insurance, short and long-term disability, and employee assistance programs.                    /div>                /div>            /div>            div classcareers-card>                div classcareers-card-title>                    Time Off                /div>                div classcareers-card-body>                    img srcimages/careers/downarrow.png altcard down arrow onclickRevealCard(cardTwo)>                    div classcareers-card-body-paragraph idcardTwo>                        img srcimages/careers/uparrow.png altcard up arrow onclickHideCard(cardTwo)>                        br>br>                        We believe in balance and provide generous time off for all employees to include a minimum of 3 weeks of accrued vacation, paid sick leave, 10 paid holidays and an annual Company shutdown between Christmas Day and New Years Day. Additionally, Neomorph provides comprehensive leave programs including paid maternity and parental leave for our new parents to bond with their children.                    /div>                /div>            /div>            div classcareers-card>                div classcareers-card-title>                    Total Rewards                /div>                div classcareers-card-body>                    img srcimages/careers/downarrow.png altcard down arrow onclickRevealCard(cardThree)>                    div classcareers-card-body-paragraph idcardThree>                        img srcimages/careers/uparrow.png altcard up arrow onclickHideCard(cardThree)>                        br>br>                        We offer a highly competitive compensation package to include salary, and bonus. Our employees are what makes Neomorph successful, and we believe in employee ownership. As part of our compensation package, all full-time employees are provided company stock options.                    /div>                /div>            /div>        /div>        div classcareers-categories>            div classcareers-categories-title>                h4>Research Organization/h4>            /div>            div classcareers-categories-dropdowns>                div classcareers-category>                    div classcareers-category-title idcat1title>                        div classcareers-category-title-text>                            Biology                        /div>                        div classcareers-category-title-image>                            img srcimages/careers/downarrow.png altcategory down arrow onclickcatShow(cat1)>                        /div>                    /div>                    div classcareers-category-paragraph idcat1 styledisplay:none;>                        h4>Biology/h4>                        div classcareers-category-paragraph-text>                            The Biology department at Neomorph consists of established expertise in the targeted protein degradation space, enabling comprehensive target discovery as well as rigorous drug optimization.  Working collaboratively with all other departments at Neomorph, the Biology Department strives to identify effective therapeutics across multiple disease areas.                        /div>                        div classcareers-category-paragraph-image>                            img srcimages/careers/uparrow.png altcategory up arrow onclickcatHide(cat1)>                        /div>                    /div>                /div>                div classcareers-category>                    div classcareers-category-title idcat2title>                        div classcareers-category-title-text>                            Pharmacology                        /div>                        div classcareers-category-title-image>                            img srcimages/careers/downarrow.png altcategory down arrow onclickcatShow(cat2)>                        /div>                    /div>                    div classcareers-category-paragraph idcat2 styledisplay:none;>                        h4>Pharmacology/h4>                        div classcareers-category-paragraph-text>                            The Pharmacology department at Neomorph is a fully enabled group, working closely with Biology and Chemistry to provide early in vivo target validation as well as advancing drug discovery projects through lead optimization efforts.  The department is comprised of experts in preclinical animal modeling in various disease areas.                        /div>                        div classcareers-category-paragraph-image>                            img srcimages/careers/uparrow.png altcategory up arrow onclickcatHide(cat2)>                        /div>                    /div>                /div>                div classcareers-category>                    div classcareers-category-title idcat3title>                        div classcareers-category-title-text>                            Molecular Sciences                        /div>                        div classcareers-category-title-image>                            img srcimages/careers/downarrow.png altcategory down arrow onclickcatShow(cat3)>                        /div>                    /div>                    div classcareers-category-paragraph idcat3 styledisplay:none;>                        h4>Molecular Sciences/h4>                        div classcareers-category-paragraph-text>                            The Molecular Sciences department at Neomorph has deep expertise in protein chemistry, X-ray crystallography, Cryo-EM, chemical biology, and proteomics approaches for targeted protein degradation drug discovery. Molecular Sciences aims to enable project teams with molecular and structural understanding of our therapeutics while working to open new horizons in targeted protein degradation technologies.                        /div>                        div classcareers-category-paragraph-image>                            img srcimages/careers/uparrow.png altcategory up arrow onclickcatHide(cat3)>                        /div>                    /div>                /div>                div classcareers-category>                    div classcareers-category-title idcat5title>                        div classcareers-category-title-text>                            Lead Discovery                        /div>                        div classcareers-category-title-image>                            img srcimages/careers/downarrow.png altcategory down arrow onclickcatShow(cat5)>                        /div>                    /div>                    div classcareers-category-paragraph idcat5 styledisplay:none;>                        h4>Lead Discovery/h4>                        div classcareers-category-paragraph-text>                            The Lead Discovery team at Neomorph consists of experienced high-throughput screening (HTS) and automation experts looking to push the boundaries of sensitivity and efficiency. Working closely with other teams at Neomorph, allows the identification of novel chemical matter and broadly profile therapeutic leads.                        /div>                        div classcareers-category-paragraph-image>                            img srcimages/careers/uparrow.png altcategory up arrow onclickcatHide(cat5)>                        /div>                    /div>                /div>                div classcareers-category>                    div classcareers-category-title idcat6title>                        div classcareers-category-title-text>                            Medicinal Chemistry                        /div>                        div classcareers-category-title-image>                            img srcimages/careers/downarrow.png altcategory down arrow onclickcatShow(cat6)>                        /div>                    /div>                    div classcareers-category-paragraph idcat6 styledisplay:none;>                        h4>Medicinal Chemistry/h4>                        div classcareers-category-paragraph-text>                            The Medicinal Chemistry department at Neomorph has established unique molecular glue designs to allow sampling of broad target space. Progressing these efforts, enabled by close collaboration with colleagues across departments, has driven the development of effective therapeutics against difficult to drug targets.                        /div>                        div classcareers-category-paragraph-image>                            img srcimages/careers/uparrow.png altcategory up arrow onclickcatHide(cat6)>                        /div>                    /div>                /div>                div classcareers-category>                    div classcareers-category-title idcat7title>                        div classcareers-category-title-text>                            Data Sciences                        /div>                        div classcareers-category-title-image>                            img srcimages/careers/downarrow.png altcategory down arrow onclickcatShow(cat7)>                        /div>                    /div>                    div classcareers-category-paragraph idcat7 styledisplay:none;>                        h4>Data Sciences/h4>                        div classcareers-category-paragraph-text>                            The Data Science department at Neomorph establishes computational and informatics capabilities to support advanced analytics and cross team collaboration. This includes developing cross team data strategy, automated data workflows, bioinformatics pipelines, cutting edge visualizations and machine learning technologies.                        /div>                        div classcareers-category-paragraph-image>                            img srcimages/careers/uparrow.png altcategory up arrow onclickcatHide(cat7)>                        /div>                    /div>                /div>            /div>        /div>    /div>    !--p>©Neomorph 2026. Powered by a hrefhttps://www.saberin.com/>Saberin Design/a>/p>-->/div>        !-- Contact page -->        div classcontact-content screen hidden idcontact>    div classcontact-header>        h1>Contact/h1>    /div>    div idContactFormWrapper>        p classcontact-form-error text-red styledisplay: none;>Error sending form, ensure all fields are filled out. Please try again. /p>        form idContactForm>            div classcontact-row>                div classcontact-field>                    input idFirstName classinput-field typetext placeholderFirst Name required />                /div>                div classcontact-field>                    input idLastName classinput-field typetext placeholderLast Name required />                /div>                div classcontact-field>                    input idEmail classinput-field typeemail placeholderEmail required />                /div>            /div>            div classcontact-row>                div classcontact-field>                    textarea idMessage classinput-field placeholderComments required>/textarea>                /div>            /div>            div classcontact-submit>                div classsubmit>                    div classcaptcha>                        div classg-recaptcha data-callbackrecaptchaCallback data-sitekey6LcJGWshAAAAAHz7p0WHysb1eL0bESGvKhEPhdFQ>/div>                        !-- add in data recaptcha site key for each new site created-->                        div classsubmit-button-div>                            button idSubmitButton typebutton classbtn btn-primary formSend onclickcreateEmail(this) disabled>Submit/button>                        /div>                    /div>                /div>                div classcol-lg-4 col-12 idformError>                    div>/div>                /div>            /div>        /form>    /div>/div>script>  function recaptchaCallback(){    $(#SubmitButton).attr(disabled, false);  }/script>        !--Cannot contain screen class (screen class is needed on each page for search functionality)-->        div classsearch-results fade-in-delayed hidden idSearchResults>        /div>        div classsocialMediaButtons fade-in-delayed>            a target_blank hrefhttps://www.linkedin.com/company/neomorph-llc>img stylewidth:30px;margin-right:15px;cursor:pointer; srcimages/header/linkedin_icon3x.png>/a>            a target_blank hrefhttps://twitter.com/neomorphinc>img stylewidth:30px;cursor:pointer; srcimages/header/x-social-media-blueicon.svg>/a>        /div>        div classcopyright fade-in-delayed>            p>                ©Neomorph 2026. Powered by a classfooter-link hrefhttps://www.saberin.com target_blank>Saberin Design/a> | a classfooter-link hrefprivacy.html>Privacy Policy/a> | a classfooter-link hrefterms.html>Terms of Service/a>            /p>        /div>    /main>/div>script>	(function() {		var elements;		var windowHeight;		var isScrolling  false;		document.querySelector(video).playbackRate0.5;		function init() {			elements  document.querySelectorAll(.hidden);			windowHeight  window.innerHeight;			setPage();			var headerLogoWidth  $(.header-logo img).width();			$(.home-img-wrapper).css(borderRadius,headerLogoWidth);          setTimeout(function(){            $(.home-img-wrapper > styleopacity: 0).removeAttr(style);            $(.home-text-wrapperstyleopacity: 0).removeAttr(style);          }, 500)		}		function setPage(){			var section  window.location.href.split(#)1;			if(section   || section  undefined)				section  home			if(section ! home){              $(#home).addClass(hidden);            }			$(#link + section).trigger(click);		}		$(.scroll-button).on(click, function(){			$(#linkabout).trigger(click);		});		// window.addEventListener(scroll, checkPosition);		$(window).on(wheel, function(event){			if(isScrolling)				return;			isScrolling  true;			setTimeout(function(){				isScrolling  false;			}, 1000)			// If section of page is scrollable text do no change page			if($(.about-content).not(.hidden).length > 0 && $(.about-paragraph p).is(:hover))				return;			if($(.science-content).not(.hidden).length > 0 && $(.science-paragraph).is(:hover))				return;			if($(.news-content).not(.hidden).length > 0 && $(.news-article).is(:visible))				return;			if($(.news-content).not(.hidden).length > 0 && $(.news-articles).is(:hover))				return;            if($(.careers-content).not(.hidden).length > 0 && $(.careers-paragraph).is(:hover))                return;            if($(.leadership-content).not(.hidden).length > 0 && $(.leadership-profile-view).is(:hover))                return;            if($(.leadership-content).not(.hidden).length > 0 && $(.leadership-profiles).is(:hover))                return;			// if($(.leadership-content).not(.hidden).length > 0){			// 	var leaderBioSection  $(.leadership-profile-view);			// 	for(var i  0; i  leaderBioSection.length; i++){			// 		if($(leaderBioSectioni).is(:hover))			// 			return;			// 	}			// }			// disabled scroll on search result screen			if($(.search-results).not(.hidden).length > 0)				return;			if(event.originalEvent.deltaY  0){				//wheeled up				$($($($(li a.selected)0).parent(li).prev(li)0).children(a)0).trigger(click)			}			else{				//wheeled down				$($($($(li a.selected)0).parent(li).next(li)0).children(a)0).trigger(click)			}		});		window.addEventListener(resize, init);		init();	})();	function mobileChangePage(location){		$(#link + location).trigger(click);	}	function changePage(obj){		var section  $(obj).data(ref);		var sectionDiv  $(`.${section}-content`);		var previousSectionDiv  $(.screen).not(.hidden);		var fadeType  fade-in-element;		if(section  home) {			fadeType  home-fade-in-animation			setHomeLogoPosition();		}		var delay  0;		var urlSection  window.location.href.split(#)1;		if($(previousSectionDiv).attr(id)  home && section ! home && urlSection  home){			$(.home-img-wrapper).addClass(home-logo-leave-anim)			fadeType  fade-in-element-delayed			delay  800;			$(.home-img-wrapper div).hide();			$(.transition-img).show();			if($(document).width()  1024){				delay  0;				$(.transition-img).hide();			}			$(.home-text-wrapper).fadeOut(delay);			var newWidth  $(.header-logo img)0.naturalWidth/ ($(.header-logo img)0.naturalHeight / (($(body).height() * .75) - 16)) + 20			$(.transition-img).animate({				width: newWidth + px,			}, 800)		}		else{			$(.home-img-wrapper).removeClass(home-logo-leave-anim);			$(.home-text-wrapper).css(display, initial);		}		setTimeout(function(){			// display new page			if(previousSectionDiv.attr(id) ! home)				previousSectionDiv.addClass(hidden);			$(.fade-in-element).removeClass(fade-in-element);			$(.come-in).removeClass(come-in);			$(sectionDiv).addClass(fadeType).removeClass(hidden);			setHomeLogoPosition();			// update nav bar			$(a.selected).removeClass(selected);			$(`#link${section}`).addClass(selected);			$(.active-line).removeClass(active-line);			$($(`#link${section}`).siblings(.line)0).addClass(active-line);			var prevNav  $(.nav-link.selected).parent().prevAll(li);			for(var i  0; i  prevNav.length; i++){				$(prevNav).children(.line).addClass(active-line);			}			//update url			window.location  $(`#link${section}`).attr(href);			//Fixes profile bios being visible on navigation click, temp, find better way to fix issues			hideLeaderBios();			resetNewsPage();			clearContactForm();			if(section  home){				$(#header).hide();				$(#bg).hide();				$(.copyright).hide();                $(.socialMediaButtons).hide();			}			else if(previousSectionDiv.attr(id)  home) {				$(#header).fadeIn();				$(#bg).fadeIn();				$(.copyright).fadeIn();                $(.socialMediaButtons).fadeIn();				setTimeout(function(){					$(previousSectionDiv).addClass(hidden);					$(.home-img-wrapper div).show();					$(.transition-img).hide();					$(transition-img).width(300)				},800)			}			else {				$(#header).show();				$(#bg).show();				$(.copyright).show();                $(.socialMediaButtons).show();			}			if(section  leadership)				$(.management).trigger(click);			resetSearchBar();			$(#SearchResults).addClass(hidden);			$(.home-img-wrapper).css({				marginLeft: 0,				marginTop: 0			})			console.log(width:  + $(.home-img-wrapper).width())			console.log(left:  + $(.home-img-wrapper).css(left))			console.log(top:  + $(.home-img-wrapper).css(top))		}, delay)	}	function setHomeLogoPosition(){		var imgPlaceholderOffset  $(.home-img-placeholder).offset();		$(.home-img-wrapper).css({			left: imgPlaceholderOffset.left + px,			top: imgPlaceholderOffset.top + px		})	}	/*****************************************Search Feature*****************************************/	$(function(){		$(#SearchWrapper input).on(keyup, function(e) {			$(#SearchResults).html();			$(#SearchResults).append(div classsearch-result-back-button onclickhideSearchResults()>/div>)			// if search box is empty, return to page before search result page was brought up, sets focus to text box incase the users intent was to clear the textbox to start over			var text  $(this).val().toLowerCase();			if(text  ) {				$(.search-result-back-button).trigger(click);				$(#SearchWrapper input).focus();				resetSearchBar();				return;			}			// if search happened at homescreen, then fade in background and navbar			if($(.screen).not(.hidden).attr(id)  home){				$(#header).fadeIn();				$(#bg).fadeIn();				$(.copyright).fadeIn();                $(.socialMediaButtons).fadeIn();			}			// hide current screen and fade in search results			$(.screen).not(.hidden).addClass(hidden);			$(#SearchResults).addClass(fade-in-element).removeClass(hidden);			$(#SearchWrapper).css({				top: 0,				right: 0,				left: 0,				margin: auto,				width: 500px,				padding-top: 5%,				padding-left: 0			});			$(#SearchWrapper input).css({				width: 500px,				font-size: 32px			})			// set page variable and init empty result count			var pages  $(.screen);			var noResultsCount  0;			// loop through pages and match regex of input box to anything for each section/subsection			for (var i  0; i  pages.length; i++){				var html  $(pagesi).html().toLowerCase();				var regExp  new RegExp(text, gi);				var results  (html.match(regExp) || ).length;				if(results > 0) {					var page  $(pagesi).attr(id);					$(#SearchResults).append(`div classresult data-page${page} onclicksearchResultClick(this)> ${page} (${results})/div>`)					// if searching leadership, also search its bio sections for each leader, display the count separately					if(page  leadership){						var leaders  $(.leader-bio);						for(var j  0; j  leaders.length; j++){							var subResults  ($(leadersj).html().match(regExp) || ).length;							if(subResults > 0) {								var leaderName  $(leadersj).siblings(.leader-name).text();								var leaderId  $(leadersj).attr(class).split( )1								$(#SearchResults).append(`div classsub-result data-page${page} data-leader${leaderId} onclicksearchResultClick(this)> ${leaderName} (${subResults})/div>`)							}						}					}					// if searching news also search each article, display the count separately					if(page  news){						var articles  $(.news-article);						for(var k  0; k  articles.length; k++){							var subResults  ($(articlesk).html().match(regExp) || ).length;							if(subResults > 0){								var articleTitle  $($(articlesk).children(h2)0).text();								var articleId  $(articlesk).attr(id);								$(#SearchResults).append(`div classsub-result data-page${page} data-article${articleId} onclicksearchResultClick(this)> ${articleTitle} (${subResults})/div>`)							}						}					}				}				else{					// if no results for page, increase the no result count					noResultsCount++;				}			}			// if no result count is greater than the amount of pages, there are 0 results, and appends that info to the result page			if(noResultsCount > $(.screen).length){				$(#SearchResults).append(div classno search results>0 Search Results/div>)			}		})	});	// Back button for search results	function hideSearchResults(){		$(#SearchResults).addClass(hidden);		$(.nav-link.selected).trigger(click);		resetSearchBar();	}	// Clicking a search result takes you to page	function searchResultClick(data){		var page  $(data).data(page);		$(#link + page).trigger(click);		$(#SearchResults).addClass(hidden);		// takes you to specific article if it was clicked in search result		if(page  news && $(data).data(article) ! undefined){			var article  $(data).data(article);			$(.news-read-moredata-article + article + ).trigger(click);		}		// takes you to specific leader bio if it was clicked in search result		else if(page  leadership && $(data).data(leader) ! undefined){			var leader  $(. + $(data).data(leader)).siblings(.leader-profile-photo)0;			$(leader).trigger(click);		}		// clears the search box when selecting a search result		$(#SearchWrapper input).val();		resetSearchBar();	}	function resetSearchBar(){		$(#SearchWrapper).css({			top: 25px,			right: 25px,			left: auto,			margin: auto,			width: 200px,			padding-top: 0,			padding-left: 30px		});		$(#SearchWrapper input).css({			width: 200px,			font-size: 18px		})	}/script>/body>/html>

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Domain > neomorph.com

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Port 80

Port 443