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Ipsen Opts-in to Join Exelixis With Ongoing Development of Cabometyx for People Living With a Form of Thyroid Cancer, Based on Promising Interim Results


Ipsen Opts-in to Join Exelixis With Ongoing Development of Cabometyx for People Living With a Form of Thyroid Cancer, Based on Promising Interim Results
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Detailed results will be presented at the upcoming 2021 American Society of Clinical Oncology (ASCO) Annual Meeting
Participation in the collaboration will provide Ipsen with access to full trial data to support potential future regulatory submissions
Disclaimer: Intended for international media and investor audiences only
Regulatory News:
Ipsen (Euronext: IPN; ADR: IPSEY) today announced it has exercised its option to collaborate with Exelixis, Inc. (Exelixis) in the pivotal COSMIC-311 Phase III trial. COSMIC-311 is evaluating Cabometyx
(cabozantinib) 60 mg versus placebo in people living with radioiodine-refractory differentiated thyroid cancer (DTC) who have progressed after up to two prior vascular endothelial growth factor receptor (VEGFR)-targeted therapies. ....

France General , United States , Hong Kong , United Kingdom , New Zealand , South Korea , Dominican Republic , Saudi Arabia , Russian Federation , Giovanni Asta , Howard Mayer , Gemma Roper , Ipsen Euronext , Head Of Research , American Society Of Clinical Oncology , Drug Administration , Takeda Pharmaceutical Company , Global Franchise Communications , European Thyroid Association Guidelines For The Treatment , Exelixis Inc , Clinical Oncology , Annual Meeting , Executive Vice President , Breakthrough Therapy Designation , Product Characteristics , Takeda Pharmaceutical Company Limited ,

Ipsen Receives Positive CHMP Opinion Recommending Cabometyx in Combination With Opdivo as First-line Treatment for Patients Living With Advanced Renal Cell Carcinoma


Ipsen Receives Positive CHMP Opinion Recommending Cabometyx in Combination With Opdivo as First-line Treatment for Patients Living With Advanced Renal Cell Carcinoma
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Patients treated with Cabometyx in combination with Opdivo reported significantly better health-related quality of life and a lower rate of discontinuation versus sunitinib
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Regulatory News:
Ipsen (Euronext: IPN; ADR: IPSEY) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has recommended approval for Cabometyx
(cabozantinib) in combination with Bristol Myers Squibb s Opdivo
(nivolumab) for the first-line treatment of advanced renal cell carcinoma (aRCC). The European Commission, which has the authority to approve medicines for the European Union (E.U.), will now review the CHMP recommendation and a final decision on the application in the E.U. is expected in the coming months. ....

France General , United States , Hong Kong , United Kingdom , New Zealand , South Korea , United Arab Emirates , Comunidad Autonoma De Cataluna , Dominican Republic , Saudi Arabia , Russian Federation , Cristina Su , Giovanni Asta , Bristol Myers Squibb Opdivo , Howard Mayer , Ipsen Euronext , Head Of Research , American Society Of Clinical Oncology , Bristol Myers Squibb Company , Takeda Pharmaceutical Company , Exelixis Inc , European Union , Virtual Congress , Bristol Myers Squibb , Committee For Medicinal Products Human Use , American Cancer Society ,