Study identifier:D6974C00001
ClinicalTrials.gov identifier:NCT07007793
EudraCT identifier:N/A
CTIS identifier:2025-520740-16-00
A Randomised, Double-Blind, Placebo-Controlled, Parallel-Group Study to Assess the Efficacy and Safety of Baxdrostat in Adult Participants with Primary Aldosteronism
Primary hyperaldosteronism
Phase 3
No
Baxdrostat, Placebo
All
180
Interventional
18 Years - n/a
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 May 2025 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Baxdrostat Baxdrostat administered orally, once daily (QD). | Drug: Baxdrostat Baxdrostat tablet administered orally, once daily (QD). Other Name: CIN-107 |
Placebo Comparator: Placebo Matching placebo administered orally, once daily (QD). | Drug: Placebo Placebo tablet matching baxdrostat, administered orally, once daily (QD). |