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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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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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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ProMIS Neurosciences granted fast track designation by US FDA for PMN310 in the treatment of Alzheimer’s disease

21 July 2025 -  ProMIS Neurosciences today announced that the US FDA has granted fast track designation to PMN310, the ...

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Bristol Myers Squibb’s supplemental new drug application for Sotyktu (deucravacitinib) for the treatment of adults with active psoriatic arthritis accepted for review across four regions globally

21 July 2025 - Bristol Myers Squibb today announced that the US FDA has accepted for review the supplemental new ...

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Bio-Thera Solutions announces FDA accepts biologics license application for BAT2506, a proposed biosimilar to Simponi

16 July 2025 - Bio-Thera Solutions today announced that the US FDA has accepted its biologics license application for BAT2506, a ...

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Genentech provides update on supplemental biologics license application for Columvi combination for people with relapsed or refractory diffuse large B-cell lymphoma

18 July 2025 - Genentech announced today that the US FDA issued a complete response letter for Genentech’s supplemental biologics ...

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Aldeyra Therapeutics announces FDA acceptance for review of reproxalap new drug application for the treatment of dry eye disease

17 July 2025 - PDUFA target action date 16 December 2025. ...

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Johnson & Johnson receives US FDA priority review for TAR-200 NDA in high-risk non-muscle invasive bladder cancer

17 July 2025 - New drug application supported by results from the Phase 2b SunRISe-1 study. ...

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