Biopharma Transcript

Niagen Bioscience, Inc. Unknown

Nasdaq · Pre-clinical · rare genetic · small molecule · EDGAR · Updated Oct 24, 2026

Niagen Bioscience, Inc. (Nasdaq: Unknown) is a rare genetic drug developer. Its lead program, NB4168, is in Pre-clinical for Ataxia-Telangiectasia (A-T).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Pipeline

ProgramIndicationModalityStage
NB4168Ataxia-Telangiectasiasmall moleculePre-clinical

Recent results and decisions

  1. Aug 4, 2026
    approval NB4168 received Rare Pediatric Disease designation from the FDA and Orphan Medicinal Product Designation from the EMA for the treatment of Ataxia-Telangiectasia.NB4168 received the Rare Pediatric Disease (RPD) designation for the treatment of A-T from the U.S. Food and Drug Administration, and Orphan Medicinal Product Designation (OMPD) from the European Medicines Agency (EMA), supporting the Company's plans to advance the program globally. Filing
  2. Aug 4, 2026
    started Niagen Bioscience engaged Evotec as CRO for preclinical and IND enabling studies for NB4168, anticipated to begin in Q3 2026.Engaged Evotec as its contract research organization for the preclinical and IND enabling studies for NB4168, anticipated to begin in Q3 2026. Filing
  3. Aug 4, 2026
    n/a NB4168 received Rare Pediatric Disease designation from the FDA and Orphan Medicinal Product Designation from the EMA for treatment of Ataxia-Telangiectasia.NB4168 received the Rare Pediatric Disease (RPD) designation for the treatment of A-T from the U.S. Food and Drug Administration, and Orphan Medicinal Product Designation (OMPD) from the European Medicines Agency (EMA). Filing

For subscribers

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