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Efficacy, Safety, Tolerability, and Pharmacokinetics of NBIP-01435 in Adult Participants With Classic Congenital Adrenal Hyperplasia (CAH)

StatusNot Yet Recruiting
PhasePhase 2
Started2026-12-01
View on ClinicalTrials.gov ↗
The main objective of this study is to evaluate the efficacy of different dose levels of NBIP-01435 on reducing elevated androstenedione (A4) levels in adults with classic CAH.
Trial Details
NCT Number NCT07850739
Lead Sponsor Neurocrine Biosciences
Conditions Congenital Adrenal Hyperplasia
Enrollment 36 participants
Start Date 2026-12-01
Primary Completion 2028-03-16 (estimated)
Study Completion 2028-05-11 (estimated)
Updated on ClinicalTrials.gov 2026-09-30