kite pharma pipeline

© 2020 Gilead Sciences, Inc. All rights reserved. DLBCL: Diffuse large B-cell lymphoma. 2 Expected submission and/or approvals in 2021. ALL - Acute lymphocytic leukemia. The deal for Kite would be one of Gilead’s biggest, more than the $11 billion purchase of liver-disease drugmaker Pharmasset in 2012, which provided Gilead with hepatitis C therapies that are among the world’s top-selling drugs. CLL: Chronic lymphocytic leukemia. “The acquisition of Kite establishes Gilead as a leader in cellular therapy and provides a foundation from which to drive continued innovation for people with advanced cancers,” said John F. Milligan, PhD, Gilead’s President and Chief Executive Officer. Our similar cultures and histories of driving rapid innovation in order to bring more effective and safer products to as many patients as possible make this an excellent strategic fit.”. Please enter your username or email address. Brexu-cel - brexucabtageneautoleucel, formerly KTE-X19. CAR-T is different from typical small molecule or biologic therapies because it is manufactured for each individual patient using their own cells. MCL: Mantle cell lymphoma. Lost your password? Kite’s most advanced therapy candidate, axicabtagene ciloleucel (axi-cel), is a CAR T therapy currently under priority review by the U.S. Food and Drug Administration (FDA). These uses have not been approved by the US Food and Drug Administration or other regulatory authorities. Kite Pharma is a development-stage biotechnology company designing and developing immune-based therapies to treat cancer indications. Axi-cel- Axicabtagene Ciloleucel. ... Report Celebrating Transgender Awareness Week Kite Pharma Harnessing The Immune System ... KITE-718 (MAGE-A3/A6) Solid tumor. Gilead’s research and development program is focused on what’s next. Although the approval seems pretty certain, there has been questions about whether Kite could capitalize on the treatment before competition hits the market. Some of the content on this page is not intended for users outside the US. There is no guarantee that these therapies or uses will be commercialized. The safety and efficacy of these investigational agents or investigational uses of marketed products have not been established. NDA/BLA/MAA, P3 and Registrational P2 Trials, NMEs via In-Licensing, Options, and Product Acquisitions. “The field of cell therapy has advanced very quickly, to the point where the science and technology have opened a clear path toward a potential cure for patients. For the latest updates on our ongoing response to COVID-19, please, Clinical Trials Transparency & Data Sharing Policy, Gilead Sciences Statement on the Solidarity Trial, Statement from Brett Pletcher on Gilead Sciences Settlement Over Charitable Donations, Gilead Remains Committed to Maintaining Advancing Access® Program for HIV Prevention and Treatment Medicines, Gilead Sciences Update on Veklury® (Remdesivir) Manufacturing Network, Gilead Sciences Statement on State Attorneys General Letter on Remdesivir, Gilead Sciences Statement on the Initiation of Clinical Testing of an Inhaled Solution of Remdesivir for Potential Outpatient Treatment of COVID-19, Gilead Sciences Statement on Phase 2/3 Clinical Trial of Remdesivir in Pediatric Patients Hospitalized With COVID-19, Gilead Sciences Statement on Remdesivir Clinical Data, Gilead Sciences Response to U.S.

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