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ClinicalTrials.gov record
Active, not recruiting Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT03604198

Public ClinicalTrials.gov record NCT03604198. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 9:12 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label Extension Study of the Safety of Relacorilant (CORT125134) in the Treatment of the Signs and Symptoms of Endogenous Cushing Syndrome

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT03604198
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Corcept Therapeutics
Industry
Enrollment
125 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
Not listed
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 7, 2018 (Actual)
Primary completion
Dec 2026 (Estimated)
Completion
Dec 2026 (Estimated)
Last update posted
Oct 9, 2026

2018 – 2026

United States locations

U.S. sites
25
U.S. states
19
U.S. cities
24
Facility City State ZIP Site status
Site 49 Phoenix Arizona 85013 —
Site 35 Stanford California 94305 —
Site 39 Torrance California 90502 —
Site 50 Miami Florida 33136 —
Site 10 Atlanta Georgia 30318 —
Site 9 Chicago Illinois 60611 —
Site 1 Indianapolis Indiana 46202 —
Site 5 Metairie Louisiana 70006 —
Site 27 Baltimore Maryland 21287 —
Site 13 Fall River Massachusetts 02721 —
Site 8 Ann Arbor Michigan 48109 —
Site 36 Rochester Minnesota 55905 —
Site 34 Jackson Mississippi 39202 —
Site 3 St Louis Missouri 63110 —
Site 55 Reno Nevada 89511 —
Site 6 Albany New York 12206 —
Site 24 New York New York 10021 —
Site 4 Wilmington North Carolina 28401 —
Site 43 Cleveland Ohio 44195 —
Site 2 Pittsburgh Pennsylvania 15212 —
Site 46 Pittsburgh Pennsylvania 15213 —
Site 11 Dallas Texas 75390 —
Site 7 El Paso Texas 79935 —
Site 32 Fort Worth Texas 76132 —
Site 12 Houston Texas 77079 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 23 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03604198, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 9, 2026 · Synced Oct 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03604198 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →