US FDA approves updated indication for Winrevair (sotatercept-csrk) in adults with pulmonary arterial hypertension (WHO Group 1 pulmonary hypertension) based on Phase 3 ZENITH study

27 October 2025 - Merck today announced that the US FDA has approved an update to the US product label based ...

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Lilly's Omvoh (mirikizumab-mrkz) approved by US FDA as a single-injection maintenance regimen in adults with ulcerative colitis

27 October 2025 - Omvoh now offers patients a simplified maintenance experience with one monthly injection, replacing the previous two injection ...

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Receipt of complete response ketter from US FDA for investigational ND0612

23 October 2025 - Mitsubishi Tanabe Pharma today announced that the US FDA has issued a complete response letter for ...

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Bayer’s Lynkuet (elinzanetant) approved in the US for treatment of moderate to severe vasomotor symptoms due to menopause

24 October 2025 - This approval is supported by data from the Phase 3 OASIS clinical program evaluating Lynkuet (elinzanetant) for ...

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FDA approves revumenib for relapsed or refractory acute myeloid leukaemia with a susceptible NPM1 mutation

24 October 2025 - Today, the FDA approved revumenib (Revuforj, Syndax Pharmaceuticals), a menin inhibitor, for relapsed or refractory acute ...

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Sydnexis receives complete response letter from FDA for SYD-101 to slow paediatric myopia progression

23 October 2025 - Sydnexis, today announced that the US FDA has issued a complete response letter for the new ...

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FDA approves belantamab mafodotin-blmf for relapsed or refractory multiple myeloma

23 October 2025 - Today, the FDA approved belantamab mafodotin-blmf (Blenrep, GlaxoSmithKline), a B-cell maturation antigen (BCMA)-directed antibody and microtubule ...

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Glaukos announces FDA approval of Epioxa

20 October 2025 - Epioxa expected to be commercially available in Q1, 2026. ...

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FDA approves Roche’s Gazyva/Gazyvaro for the treatment of lupus nephritis

20 October 2025 - FDA approval based on superiority of Gazyva/Gazyvaro over standard therapy alone, as shown in Phase 2 NOBILITY ...

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Xbrane provides regulatory update on FDA review of its ranibizumab biosimilar candidate

19 October 2025 - Xbrane Biopharma announce that the US FDA has issued a complete response letter to the Company’s biologics ...

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Azurity Pharmaceuticals announces the FDA approval of Ferabright (ferumoxytol injection), the first and only iron-based contrast agent indicated for magnetic resonance imaging of the brain

17 October 2025 - Azurity Pharmaceuticals announced today that the US FDA has approved Ferabright (ferumoxytol injection), the first and only ...

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FDA approves Novo Nordisk's oral semaglutide for cardiovascular risk reduction in adults with type 2 diabetes who are at high risk, including those who have not had a prior CV event

17 October 2025 - In the SOUL trial, oral semaglutide 14 mg reduced the risk of MACE by 14% compared to ...

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Tezspire approved in the US for chronic rhinosinusitis with nasal polyps

17 October 2025 - AstraZeneca and Amgen’s Tezspire (tezepelumab) has been approved in the US for the add-on maintenance treatment of ...

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Roche's Elecsys pTau181 becomes the only FDA cleared blood test for use in primary care to rule out Alzheimer's related amyloid pathology

13 October 2025 - Roche today announced that the US FDA has cleared its Elecsys pTau181 test, the only blood ...

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US FDA approves updated indication statement for Rinvoq (upadacitinib) for the treatment of inflammatory bowel disease

13 October 2025 - Updated indication allows the use of Rinvoq (upadacitinib) prior to the use of tumour necrosis factor blocking ...

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