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Completed Phase 3 Interventional Results available

A Study of the Efficacy and Safety of Relacorilant in Patients With Endogenous Cushing Syndrome

ClinicalTrials.gov ID: NCT03697109

Public ClinicalTrials.gov record NCT03697109. 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 21, 2026, 6:39 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

Glucocorticoid Receptor Antagonism in the Treatment of Cushing Syndrome (GRACE): A Phase 3, Double-Blind, Placebo-Controlled, Randomized-Withdrawal Study of the Efficacy and Safety of Relacorilant

Brief summary

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

This is a Phase 3, double-blind, placebo-controlled, randomized-withdrawal study to assess the efficacy, safety and pharmacokinetics (PK) of relacorilant in patients with endogenous Cushing syndrome and concurrent type 2 diabetes mellitus/impaired glucose tolerance (DM/IGT) and/or uncontrolled hypertension (HTN).

Study identification

NCT ID
NCT03697109
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Corcept Therapeutics
Industry
Enrollment
152 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 80 Years
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
Nov 15, 2018 (Actual)
Primary completion
Apr 8, 2024 (Actual)
Completion
Apr 15, 2024 (Actual)
Last update posted
Jul 16, 2025

2018 – 2024

United States locations

U.S. sites
32
U.S. states
22
U.S. cities
29
Facility City State ZIP Site status
Site 21 Phoenix Arizona 85013 —
Site 36 Los Angeles California 90095 —
Site 68 Torrance California 90502 —
Site 10 Miami Florida 33136 —
Site 14 Atlanta Georgia 30318 —
Site 41 Chicago Illinois 60611 —
Site 7 Indianapolis Indiana 46202 —
Site 2 Metairie Louisiana 70006 —
Site 45 Baltimore Maryland 21205 —
Site 46 Boston Massachusetts 02115 —
Site 20 Ann Arbor Michigan 48109 —
Site 4 Jackson Mississippi 39202 —
Site 13 St Louis Missouri 63110 —
Site 53 Omaha Nebraska 68198 —
Site 72 Reno Nevada 89511 —
Site 8 Albany New York 12203 —
Site 6 Jamaica New York 11432 —
Site 57 New York New York 10021 —
Site 35 New York New York 10029 —
Site 39 New York New York 10065 —
Site 1 Wilmington North Carolina 28401 —
Site 17 Columbus Ohio 43210 —
Site 11 Oklahoma City Oklahoma 73104 —
Site 62 Philadelphia Pennsylvania 19107 —
Site 19 Pittsburgh Pennsylvania 15212 —
Site 71 Pittsburgh Pennsylvania 15213 —
Site 5 Summerville South Carolina 29485 —
Site 51 Dallas Texas 75390 —
Site 3 El Paso Texas 79935 —
Site 65 Houston Texas 77079 —
Site 56 Shavano Park Texas 78231 —
Site 31 Everett Washington 98201 —

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 32 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03697109, 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 Jul 16, 2025 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03697109 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →