A comprehensive view of European Medicines Agency (EMA). This page highlights a small sample of our full coverage.
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CHMP adopts positive opinion recommending approval of Bristol Myers Squibb’s Opdivo nivolumab in combination with Cisplatin and Gemcitabine for the first-line treatment of adult patients with unresectable or metastatic urothelial carcinoma
Published:
April 26, 2024
by Bristol-Myers Squibb Co.
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Phase 3 study of Roche's OCREVUS subcutaneous injection shows near-complete suppression of multiple sclerosis relapse activity and lesions; approval anticipated from FDA and EMA in 2024
Published:
April 17, 2024
by F. Hoffmann-La Roche Ltd. (Roche)
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Bristol-Myers Squibb receives EMA's positive opinion on anemia therapy, bolsters collaborative health initiatives, and continues technological advancement in disease treatment
Published:
February 24, 2024
by Industry Intelligence Inc.
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FDA grants priority review to Regeneron's BLA for linvoseltamab as a treatment for multiple myeloma, decision date is set for August 22, 2024; European medicines agency accepted the drug for review earlier this month
Published:
February 21, 2024
by Regeneron Pharmaceuticals Inc.
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Bristol Myers announces acceptance of US and EU regulatory filings for neoadjuvant opdivo (nivolumab) and chemotherapy followed by surgery and adjuvant opdivo in resectable non-small cell lung cancer
Published:
February 07, 2024
by Bristol-Myers Squibb Co.
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