Extension Study to Evaluate the Safety of Long-Term Use of Relacorilant in Patients With Cushing Syndrome

Running, not enrolling · Phase 2

Conditions studied: Cushing Syndrome

In brief

This is an open-label extension study to evaluate the long-term safety of relacorilant in patients with endogenous Cushing syndrome who successfully completed participation in a Corcept-sponsored study of relacorilant and may benefit from continuing treatment.

Key facts

Study ID
NCT03604198
Run by
Corcept Therapeutics
People needed
125
Starts
2018-05-07
Expected to finish
2026-12-01
Last updated by the study team
2026-04-21

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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