ClinicalTrials.gov record
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 May 19, 2026, 8:32 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

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

  • Placebo Other
  • Relacorilant Drug

Other · Drug

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 14, 2018
Primary completion
Apr 7, 2024
Completion
Apr 14, 2024
Last update posted
Jul 15, 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 15, 2025 · Synced May 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 protocol, eligibility criteria, and contact information for NCT03697109 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →