Imfinzi granted priority review and breakthrough therapy designation in the US for patients with resectable early-stage gastric and gastro-oesophageal junction cancers

28 July 2025 - Based on MATTERHORN Phase 3 trial results which demonstrated a statistically significant and clinically meaningful event-free survival ...

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Sobi announces US FDA approves Doptelet (avatrombopag) for the treatment of thrombocytopenia in paediatric patients one year and older with persistent or chronic immune thrombocytopenia

25 July 2025 - The primary outcome was met in 27.8% of patients, confirming the efficacy in children and adolescents ...

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Shanton receives fast track designation from US FDA for refractory gout program

25 July 2025 - Shanton Pharma today announced that FDA has designated its Investigational new drug SAP-001 as a fast track ...

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Bayer provides regulatory update on elinzanetant in the US

25 July 2025 - Bayer today announced that the US FDA has notified the company that it has extended the ...

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FDA grants priority review for Addyi (flibanserin) paving the way for expanded access to treat low sexual desire in post-menopausal women

24 July 2025 -  Sprout Pharmaceuticals today announced that the US FDA has granted priority review for its supplemental application ...

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Verastem Oncology granted fast track designation for VS-7375 for the treatment of KRAS G12D mutated locally advanced or metastatic pancreatic cancer

24 July 2025 - Enrollment is on-going in US Phase 1/2a trial for VS-7375, an oral KRAS G12D (ON/OFF) inhibitor, ...

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Commissioner's National Priority Voucher Pilot Program

22 July 2025 - Accelerated drug review for companies supporting US national interests. ...

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Avidity Biosciences receives FDA breakthrough therapy designation for delpacibart zotadirsen for the treatment of DMD in people with mutations amenable to exon 44 skipping

23 July 2025 - On track for planned BLA submission for delpacibart zotadirsen at year end 2025. ...

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Anzupgo (delgocitinib) cream is now the first and only FDA approved treatment for moderate to severe chronic hand eczema in adults

23 July 2025 - In Phase 3 clinical trials, patients experienced significant skin clearance along with marked relief from pain and ...

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Revolution Medicines announces FDA breakthrough therapy designation for elironrasib

23 July 2025 - Designation based on encouraging clinical data observed with elironrasib in patients with advanced KRAS G12C non-small ...

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Solid Biosciences receives FDA fast track designation for SGT-501 first in class gene therapy for catecholaminergic polymorphic ventricular tachycardia

23 July 2025 - SGT-501 has now received FDA fast track, orphan drug and rare paediatric disease designations. ...

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GSK announces extension of US FDA an review period for Blenrep (belantamab mafodotin-blmf) in relapsed/refractory multiple myeloma

23 July 2025 - New PDUFA date scheduled for 23 October 2025. ...

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DualityBio's next generation HER3 ADC DB-1310 granted FDA fast track designation

21 July 2025 - DualityBio announced that the US FDA has granted fast track designation to its next-generation HER3 targeting antibody ...

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Replimune receives complete response letter from FDA for RP1 biologics license application for the treatment of advanced melanoma

23 July 2025 - Replimune Group today announced that the US FDA has issued a complete response letter regarding the ...

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Johnson & Johnson seeks first icotrokinra US FDA approval aiming to revolutionise treatment paradigm for adults and adolescents with plaque psoriasis

21 July 2025 - Icotrokinra is a first in class investigational targeted oral peptide that selectively blocks the IL-23 receptor. ...

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