Clinical trial
A Double-blind, Randomised, 30-week Placebo-controlled Phase IV Study to Assess the Efficacy and Safety of Osilodrostat in Patients With Hypertension Caused by Hypercortisolaemia Due to Cushing's Syndrome
NCT07247162 is registered in ClinicalTrials.gov with RECORDATI GROUP as lead sponsor.
Search trials, sites, companies and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.
Registry record
As filed in ClinicalTrials.gov.
- Title
- A Double-blind, Randomised, 30-week Placebo-controlled Phase IV Study to Assess the Efficacy and Safety of Osilodrostat in Patients With Hypertension Caused by Hypercortisolaemia Due to Cushing's Syndrome
- Lead sponsor
- RECORDATI GROUP
- Phase
- Phase 4
- Overall status
- Not yet recruiting
- Start date
- August 31, 2026
- Completion date
- July 31, 2028
- Enrollment
- 63 (estimated)
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.
cushing syndrome, hypercortisolemia, hypertension