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Legend Biotech Announces Phase 3 CARTITUDE-4 Study of CARVYKTI (ciltacabtagene autoleucel) Has Met Its Primary Endpoint in the Treatment of Patients with Relapsed and Refractory Multiple Myeloma

27.01.2023 - Legend Biotech Corporation (NASDAQ: LEGN) (Legend Biotech), a global biotechnology company developing, manufacturing and commercializing novel therapies to treat life-threatening diseases, announced today that CARTITUDE-4, the Phase 3 study ...
United States New Jersey Hemophagocytic Lymphohistiocytosis Lida Pacaud American Society Of Clinical Oncology Janssen Biotech Inc

West Virginia sued for its ban of abortion pill

A company that makes an abortion pill filed a lawsuit Wednesday morning challenging the constitutionality of a state ban on the medication, one in what is expected to be a wave of cases arguing that the federal Food and Drug Administrations approval of the pill takes precedence over such restrictive state laws.
New York United States North Carolina University Of North Carolina West Virginia Amy Bryant

FDA Approval Mifepristone REMS Program Modification Expands Patient Access to Abortion Care | Sheppard Mullin Richter & Hampton LLP

The Food and Drug Administration (the “FDA”) has approved a modification to the Mifepristone Risk Evaluation and Mitigation Strategy (“REMS”) Program, increasing the accessibility of...
United States Jackson Women Health Organization Drug Administration Sheppard Mullin Richter Hampton Maryland Us District Court Us Supreme Court

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FDA Approves Changes to REMS Program

The FDA approved a modification to the Mifepristone Risk Evaluation and Mitigation Strategy, REMS, Program. The FDA’s approval of commercial dispensing of mifepristone likely will not change the current practice of prescribing and dispensing mifepristone for abortion.
United States Jackson Women Health Organization Drug Administration Maryland Us District Court Us Supreme Court American College Of Obstetricians

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