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

Part of paid clinical trials in Phoenix, Arizona.

Sponsor
Corcept Therapeutics
Study ID
NCT03604198
Phase
PHASE2
Status
Active Not Recruiting

Conditions

  • Cushing Syndrome

Eligibility Criteria

Sex
ALL
Age
N/A - N/A
Healthy Volunteers
Not accepted

Interventions

  • relacorilant — DRUG
    CORT125134 is supplied as capsules for oral dosing.

Study Details

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 Dates

First listed
Jul 27, 2018
Start date
May 7, 2018
Status verified
Apr 2026
Primary completion
Dec 31, 2026
Completion
Dec 31, 2026

Study Design

Enrollment
125 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: relacorilant (CORT125134)

Primary Outcome Measure

Long-term safety of relacorilant [ Time Frame: 36 months ]

Locations (25)

FacilityCityStateZIPSite coordinators
Site 49PhoenixArizona85013-
Site 35StanfordCalifornia94305-
Site 39TorranceCalifornia90502-
Site 50MiamiFlorida33136-
Site 10AtlantaGeorgia30318-
Site 9ChicagoIllinois60611-
Site 1IndianapolisIndiana46202-
Site 5MetairieLouisiana70006-
Site 27BaltimoreMaryland21287-
Site 13Fall RiverMassachusetts02721-
Site 8Ann ArborMichigan48109-
Site 36RochesterMinnesota55905-
Site 34JacksonMississippi39202-
Site 3St LouisMissouri63110-
Site 55RenoNevada89511-
Site 6AlbanyNew York12206-
Site 24New YorkNew York10021-
Site 4WilmingtonNorth Carolina28401-
Site 43ClevelandOhio44195-
Site 2PittsburghPennsylvania15212-
Site 46PittsburghPennsylvania15213-
Site 11DallasTexas75390-
Site 7El PasoTexas79935-
Site 32Fort WorthTexas76132-
Site 12HoustonTexas77079-

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