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Beigene Corporate Brochure

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Beigene Corporate Brochure The BeiGene Story A global biopharmaceutical innovator focused on improving 3,400+ 10 offices Trials in 35 treatment outcomes and patient access employees on 4 continents countries and regions (as of January 29, 2020) BeiGene is a fully-integrated biopharmaceutical Our broad product portfolio and pipeline include: company co-founded in 2010 by John Oyler, an • 3 wholly owned late-stage oncology candidates, American entrepreneur, and Dr. Xiaodong Wang, including one approved in the U.S. and one one of the youngest ever U.S. Academy of Science approved in China members and Director of China’s National Institute • 27 Phase 3 or potentially registration-enabling of Biological Sciences (NIBS) in Beijing. The two set trials ongoing, 60+ studies in total out to build a unique company that was globally • 32 clinical or commercial stage assets including focused from its inception. seven internally developed and 25 in-licensed BeiGene (NASDAQ: BGNE; HKEX 06160) focuses on BeiGene has built a strong innovative pipeline of developing novel cancer therapies where there is clinical drug candidates through internal discovery global unmet need. and collaborations. Transformative Collaboration with Amgen This global strategic oncology collaboration expands • Companies jointly developing 20 Amgen access to important oncology medicines for patients oncology pipeline assets globally, with BeiGene in China and around the globe with: leading development in China • BeiGene commercializing three Amgen oncology • Amgen investing $2.8B for a 20.5% products in China — XGEVA® (denosumab), stake in BeiGene KYPROLIS™ (carfilzomib), and BLINCYTO® (blinatumomab) BEIGENE’S COMMERCIAL PRODUCT PORTFOLIO ® • China NMPA approvals in R/R multiple myeloma and multiple myeloma BRUKINSA™ • U.S. FDA accelerated approval in November 2019 for relapsed/ refractory (R/R) REVLIMID (zanubrutinib) mantle cell lymphoma (lenalidomide) • In-licensed from Celgene (a Bristol-Myers Squibb) company, rights in China ® ABRAXANE • China NMPA approval in breast cancer Tislelizumab • China NMPA approval in R/R classical Hodgkin’s lymphoma (albumin-bound • In-licensed from Celgene (a Bristol-Myers Squibb) company, rights in China paclitaxel) • China NMPA approvals in myelodysplastic syndrome, acute myeloid leukemia, ® • China NMPA approval in giant cell tumor of bone ® XGEVA VIDAZA chronic myelomonocytic leukemia • In-licensed from Amgen, rights in China (azacitidine) (denosumab) • In-licensed from Celgene (a Bristol-Myers Squibb) company, rights in China BEIGENE’S SELECTED INVESTIGATIONAL PIPELINE1 • Investigational humanized lgG1-variant monoclonal antibody against TIM-3 • Potent second generation small molecule inhibitor of Bruton’s tyrosine kinase BGB-A425 • Currently being investigated in combination with tislelizumab in solid tumors Zanubrutinib • Currently being investigated as a monotherapy and in combination with other therapies in multiple hematologic malignancies • Investigational TIGIT monoclonal antibody BGB-A1217 • Currently being investigated as in combination with tislelizumab in solid tumors • Humanized IgG4 anti-PD-1 monoclonal antibody • Investigational small molecule Bcl-2 inhibitor Tislelizumab • Currently being investigated as a monotherapy and in combination with other therapies BGB-11417 • Currently being investigated as a monotherapy and in combination with zanubrutinib in in multiple solid tumors and hematologic malignancies hematologic malignancies • Investigational spectrum-selective kinase inhibitor of receptor tyrosine kinases, including RET, • Investigational small molecule inhibitor of PARP1 and PARP2 TAM family receptors (TYRO3, Axl, MER) and split family receptors (VEGFR2, KIT) Sitravatinib Pamiparib • Currently being investigated as a monotherapy and in combination with other therapies • Currently being investigated in combination with tislelizumab in solid tumors in multiple solid tumors • In-licensed from Mirati Therapeutics, rights in Asia ex-Japan, AU, NZ • Investigational HER2-targeted bispecific antibody • Investigational novel small molecule inhibitor with RAF monomer and dimer inhibition activities • Currently being investigated in combination with tislelizumab in solid tumors Lifirafenib • Currently being investigated as a monotherapy and in combination with mirdametinib (MEK ZW25 inhibitor from SpringWorks Therapeutics) in solid tumors • In-licensed from Zymeworks, rights in Asia ex-Japan, AU, NZ • Investigational HER2-targeted bispecific antibody drug conjugate (ADC) ZW49 • Investigational humanized monoclonal antibody against the immune checkpoint • In-licensed from Zymeworks, rights in Asia ex-Japan, AU, NZ receptor ligand PD-L1 BGB-A333 • Currently being investigated as a monotherapy and in combination with tislelizumab • Investigational KRASG12C small molecule inhibitor AMG 510 in solid tumors • In-licensed from Amgen, rights in China 1Abbreviated pipeline as of January 9, 2020. For full pipeline, visit beigene.com/science-and-product-portfolio/pipeline Meet John V. Oyler Eric Hedrick, M.D. Our Commitment Chairman, Founder & CEO Chief Advisor Members BioDuro, Galenea, Telephia, Genta, Genentech, Pharmacyclics, McKinsey & Company Epizyme BeiGene’s commitment is to never compromise of Our on the safety, compliance, or quality of our products, our research, or our services. We are focused on serving patients by delivering quality Xiaodong Wang, Ph.D. Josh Neiman Leadership drug products that consistently meet or exceed all Founder & Chairman SAB Head of U.S. Commercial NIBS: National Institute of Biological Flatiron Health, customer and regulatory requirements. Each Team Sciences in Beijing, UT Southwestern Onyx Pharmaceuticals, BeiGene employee and partner is responsible for Medical Center, Howard Hughes Genentech Medical Institute, National Academy achieving our objectives and for looking at any of Sciences BeiGene employees are opportunity where we can improve upon our high standards of performance. Xiaobin Wu, Ph.D. Guillaume Vignon, Ph.D. dedicated to translating GM of China & President SVP, Business Development groundbreaking science Pfizer, Wyeth, Bayer Merck KGaA BeiGene conducts its clinical trials in accordance with the regulatory requirements of the U.S. Food into quality innovative and Drug Administration (FDA), the European cancer therapies. Medicines Agency (EMA), and the China National Jane Huang, M.D. Lai Wang, Ph.D. Medical Products Administration (NMPA), as CMO, Hematology SVP, Head of Global Research, applicable. Likewise, BeiGene’s own state-of-the-art With a global headcount Acerta, Genentech Clinical Operation, Biometrics & APAC Clinical Development manufacturing facilities, located in China, are fully Joyant Pharmaceuticals, compliant with Good Manufacturing Practice (GMP) of over 3,400 employees, Howard Hughes Medical Institute requirements of the U.S., European and Chinese more than 1,000 are authorities and subject to inspection and approval Yong (Ben) Ben, M.D. Todd Yancey, M.D. by these authorities. It has also contracted with devoted to global clinical CMO, Immuno-Oncology SVP, Global Medical Affairs leading American and German manufacturers for BioAtla, AstraZeneca & New Market Development development and BioMarin, Clovis Oncology, production of its drug candidates. Medivation, Onyx Pharmaceuticals approximately 1,000 are in commercial operation. Our employees look forward to connecting with you to provide additional insight into BeiGene. Contact us at: 888-123-4455 or [email protected] www.beigene.com @BeiGeneUSA ©2020 BeiGene, Inc..
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