ICER releases draft evidence report on treatment for non-cystic fibrosis bronchiectasis

23 July 2025 - Public comment period now open until 19 August 2025; requests to make oral comment during public ...

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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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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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Rocket Pharmaceuticals receives FDA regenerative medicine advanced therapy designation for RP-A601 gene therapy for PKP2 arhythmogenic cardiomyopathy

17 July 2025 - -- Rocket Pharmaceuticals today announced that the US FDA has granted regenerative medicine advanced therapy designation to ...

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Genascence announces US FDA grants regenerative medicine advanced therapy designation to GNSC-001 for knee osteoarthritis

16 July 2025 - Genascence Corporation today announced that the US FDA has granted the regenerative medicine advanced therapy designation ...

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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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Praxis Precision Medicines receives FDA breakthrough therapy designation for relutrigine for the treatment of seizures associated with SCN2A and SCN8A developmental and epileptic encephalopathies

17July 2025 - The breakthrough therapy designation was granted based on the highly compelling results from the Phase 2 EMBOLD trial ...

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Pierre Fabre announces transfer of investigational new drug application for tabelecleucel from Atara Biotherapeutics

15 July 2025 - Pierre Fabre Laboratories is now responsible for all global clinical trial activities for the tabelecleucel clinical program. ...

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ICER publishes evidence report on treatments for spinal muscular atrophy

17 July 2025 - There are many remaining uncertainties around the best management of spinal muscular atrophy; ICER estimates that ...

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