A Study of the Efficacy and Safety of Relacorilant in Patients With Endogenous Cushing Syndrome
Trial details
- Registry ID
- NCT03697109
- Phase
- Phase 3
Open a linked trial to see its study details and recorded changes, or check the regulatory events below and follow their sources.
Drug identity checked against registry records
Also recorded as CORT125134
| Trial | Sponsor | Phase | Status | Primary completion |
|---|---|---|---|---|
| A Study of the Efficacy and Safety of Relacorilant in Patients With Endogenous Cushing SyndromeNCT03697109 | Corcept Therapeutics | Phase 3 | Completed | 2024-04-08Actual |
| Relacorilant With Nab-Paclitaxel and Gemcitabine in Patients With Metastatic Pancreatic AdenocarcinomaNCT07259317 | Corcept Therapeutics | Phase 2 | Recruiting | 2027-09Estimated |
| Study of Relacorilant in Combination With Nab-Paclitaxel for Patients With Recurrent Platinum-Resistant Ovarian, Fallopian Tube, or Primary Peritoneal CancerNCT03776812 | Corcept Therapeutics | Phase 2 | Completed | 2021-03-16Actual |
| A Study of the Efficacy and Safety of Relacorilant in Patients With Cortisol-Secreting Adrenal AdenomasNCT04308590 | Corcept Therapeutics | Phase 3 | Completed | 2024-09-19Actual |
| No regulatory events match this view.Try another date range or view. Events appear after automated source checks. This does not mean no FDA events have occurred. Dates that a source does not disclose stay undisclosed. |