BioRestorative receives FDA fast track designation for BRTX-100 chronic lumbar disc disease program

20 February 2025 - Reflects positive preliminary Phase 2 safety and efficacy data reported to date. ...

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World’s first potential target therapy for diffuse gastric cancer granted fast track designation by the US FDA

20 February 2025 - Signet Therapeutics announced that the US FDA has granted fast track designation for SIGX1094, the world's first ...

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Harmony Biosciences provides update on the status of the supplemental new drug application for pitolisant in idiopathic hypersomnia

19 February 2025 - Harmony Biosciences today announced that it received a refusal to file letter from the US FDA for ...

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Doron Therapeutics receives FDA regenerative medicine advanced therapy designation for Motys for treatment of symptoms associated with osteoarthritis

19 February 2025 - Doron Therapeutics today announced that the US FDA has granted regenerative medicine advanced therapy designation to ...

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PTC Therapeutics announces FDA acceptance and priority review for vatiquinone NDA for the treatment of children and adults with Friedreich's ataxia

19 February 2025 - PDUFA target action date of 19 August 2025. ...

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Fast track granted by FDA for NNZ-2591 in Pitt Hopkins syndrome

19 February 2025 - : Neuren Pharmaceuticals today announced that the US FDA has granted fast track designation for NNZ-2591 ...

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Boehringer’s zongertinib receives priority review from US FDA for the treatment of HER2 (ERBB2)-mutant advanced non-small cell lung cancer

19 February 2025 - The application for this investigational treatment is based on positive results from the Phase Ib Beamion LUNG-1, ...

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Clarity receives US FDA fast track designation for the treatment of metastatic castration resistant prostate cancer patients with copper Cu 67 SAR-bisPSMA

19 February 2025 - Clarity Pharmaceuticals is pleased to announce that the US FDA has granted fast track designation for ...

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Ultragenyx announces FDA acceptance and priority review of the biologics license application for UX111 AAV gene therapy to treat Sanfilippo syndrome type A

18 February 2025 - FDA decision expected by 18 August 2025. ...

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Petosemtamab granted breakthrough therapy designation by the US FDA for first-line PD-L1 positive head and neck squamous cell carcinoma

18 February 2025 - This marks the second breakthrough therapy designation for petosemtamab in head and neck squamous cell carcinoma. ...

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US FDA accepts Gilead’s new drug applications for twice yearly lenacapavir for HIV prevention under priority review

18 February 2025 - FDA to review applications under priority review, with a PDUFA date of 19 June 2025. ...

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Chimerix announces FDA acceptance and priority review of new drug application for dordaviprone as treatment for recurrent H3 K27M mutant diffuse glioma

18 February 2025 - PDUFA target action date of 18 August 2025. ...

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Dupixent (dupilumab) sBLA accepted for FDA priority review for the targeted treatment of bullous pemphigoid

18 February 2025 - If approved, Dupixent would be the first and only targeted medicine to treat bullous pemphigoid in the US; ...

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Rznomics liver cancer drug candidate secures fast track designation

17 February 2025 - Second fast track designation following brain cancer approval. ...

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Innovent receives second fast track designation from the US FDA for IBI363 (PD-1/IL-2α-bias bipspecific antibody fusion protein) in squamous non-small cell lung cancer

17 February 2025 - Innovent Biologics announced that its first in class PD-1/IL-2α-bias bi-specific antibody fusion protein, IBI363, has received its ...

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