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UNCY — Unicycive Therapeutics News Story

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Brief: Unicycive Therapeutics Gets Complete Response Letter From FDA On Resubmitted Oxylanthanum Carbonate NDA

BRIEF-Unicycive Therapeutics Gets Complete Response Letter From FDA On Resubmitted Oxylanthanum Carbonate NDA

- Unicycive Therapeutics Inc UNCY.O:

  • RECEIVES COMPLETE RESPONSE LETTER FROM FDA REGARDING RESUBMITTED OXYLANTHANUM CARBONATE (OLC) NEW DRUG APPLICATION (NDA)

  • FDA RAISES NO CONCERNS ON CLINICAL EFFICACY OR SAFETY DATA, NO ADDITIONAL DATA REQUESTED

  • FDA HAS NOT CONDUCTED INSPECTION OF THIRD-PARTY MANUFACTURING VENDOR FOR RESUBMITTED NDA

  • FDA CRL BASED ON THIRD-PARTY MANUFACTURING DEFICIENCIES IDENTIFIED IN JUNE 2025

  • REMAIN CONFIDENT IN EFFICACY SAFETY OF OLC; OPTIMISTIC THAT WE WILL BE ABLE TO EXPEDITIOUSLY RESUBMIT NDA

Source text: ID:nGNX3zVDRJ

Further company coverage: UNCY.O


((Reutersbriefs@thomsonreuters.com;))

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