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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...
United States Jun Saito Awny Farajallah Takeda Pharmaceutical Company Limited Drug Administration World Health Organization

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.
United States Jun Saito Awny Farajallah Drug Administration American Cancer Society Takeda Pharmaceutical Company Limited

ELAHERE® Shows Overall and Progression-Free Survival Benefit Regardless of Prior PARPi Exposure or Prior Lines of Therapy in FRα-Positive Platinum-Resistant Ovarian Cancer

Data Further Position ELAHERE to Become the New Standard of Care for Patients with FRα-Positive Platinum-Resistant Ovarian Cancer Findings to be Highlighted in Oral Presentation at ESGO Annual...
United States University Of Leuven European Society Of Gynaecological Oncology Immunogen Inc American Society Of Clinical Oncology Toon Van Gorp

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