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    • EMA Authorizes Hemophilia B Gene Therapy

      Medscape· 4 days ago

      The European Medicines Agency has given the go-ahead for Durveqtix to treat hemophilia B in adults and to Adzynma for patients with congenital thrombotic thrombocytopenic purpura.

    • Small Business - Picayune Item | Picayune Item

      The Picayune Item· 2 days ago

      CStone Announces European Medicine Agency CHMP Recommends Approval of Cejemly® (sugemalimab, anti-PD-L1) as First-Line Treatment for NSCLC PR Newswire SUZHOU, China, June 1, 2024 EMA ...