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Datopotamab deruxtecan plus IMFINZI® (durvalumab) demonstrated robust and durable tumor responses in 1st-line treatment of patients with metastatic triple-negative breast cancer in BEGONIA Phase Ib/II trial

FDA Grants Transcenta Clearance to Proceed with Global Phase III Trial of Osemitamab (TST001) as First-Line Treatment for Gastric/Gastroesophageal Cancer Patients

Takeda Provides Update on EXKIVITY® (mobocertinib)

OSAKA, Japan & CAMBRIDGE, Mass. (BUSINESS WIRE) Takeda (TSE:4502/NYSE:TAK) today announced that, following discussions with the U.S. Food and Drug Administration (FDA), it will be working with the FDA towards a voluntary withdrawal of EXKIVITY® (mobocertinib) in the U.S. for adult patients with epidermal growth fa.

Takeda Provides Update on EXKIVITY mobocertinib

Takeda TSE4502NYSETAK today announced that following discussions with the U.S. Food and Drug Administration FDA it will be working with the FDA towards a voluntary withdrawal of EXKIVITY mobocertinib in the U.S. for adult patients with epidermal growth factor receptor EGFR Exon20 ion mutationpositive ion locally advanced or metastatic nonsmall cell lung cancer NSCLC whose disease has progressed on or after platinumbased chemotherapy.

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