• FDA Approves Ocrevus (ocrelizumab) for Pediatric Patients 10 Years of Age and Older with Relapsing-Remitting Multiple Sclerosis

  Genentech, a member of the Roche Group, recently announced that the U.S. Food and Drug Administration (FDA) has approved Ocrevus (ocrelizumab) intrave···【Read More】

  Update: 21 May,2026Source: BigbearViews: 176

• FDA Approves Baxfendy (baxdrostat) as the First Aldosterone Synthase Inhibitor Treatment for Adults with Hypertension

  May 18, 2026 – Baxfendy (baxdrostat) from AstraZeneca has received FDA approval as the world's first aldosterone synthase inhibitor (ASI) for use ···【Read More】

  Update: 20 May,2026Source: BigbearViews: 217

• EU Recommends Expanding New Indications for Nivolumab (Opdivo)

  Recently, the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion recommending chan···【Read More】

  Update: 19 May,2026Source: BigbearViews: 203

• FDA Approves Immgolis (golimumab-sldi) and Immgolis Intri (golimumab-sldi) as the First Interchangeable Biosimilars to Simponi and Simponi Aria

  May 15, 2026 — The FDA has approved Immgolis (golimumab-sldi) as an interchangeable biosimilar to Simponi (golimumab), and Immgolis Intri (golimumab-s···【Read More】

  Update: 18 May,2026Source: BigbearViews: 160

• EU Approves New Expanded Indications for Dabrafenib and Trametinib!

  The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion, recommending amendmen···【Read More】

  Update: 11 May,2026Source: BigbearViews: 173