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

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

125

Participants

Timeline

Start Date

May 7, 2018

Primary Completion Date

December 31, 2025

Study Completion Date

December 31, 2025

Conditions
Cushing Syndrome
Interventions
DRUG

relacorilant

CORT125134 is supplied as capsules for oral dosing.

Trial Locations (48)

1090

Site 14, Vienna

10021

Site 24, New York

10825

Site 31, Bucharest

11863

Site 28, Bucharest

12206

Site 6, Albany

15212

Site 2, Pittsburgh

15213

Site 46, Pittsburgh

20145

Site 25, Milan

20412

Site 45, Lublin

21287

Site 27, Baltimore

28007

Site 17, Madrid

28401

Site 4, Wilmington

29006

Site 38, Málaga

30318

Site 10, Atlanta

33136

Site 50, Miami

35128

Site 48, Padua

39202

Site 34, Jackson

44195

Site 43, Cleveland

46202

Site 1, Indianapolis

48109

Site 8, Ann Arbor

55905

Site 36, Rochester

60126

Site 40, Ancona

60611

Site 9, Chicago

63110

Site 3, St Louis

64239

Site 29, Tel Aviv

70006

Site 5, Metairie

75390

Site 11, Dallas

76132

Site 32, Fort Worth

77079

Site 12, Houston

79935

Site 7, El Paso

80131

Site 21, Napoli

85013

Site 49, Phoenix

89511

Site 55, Reno

90502

Site 39, Torrance

94305

Site 35, Stanford

97080

Site 42, Würzburg

98125

Site 44, Messina

5265601

Site 20, Ramat Gan

02721

Site 13, Fall River

Unknown

Site 51, Nova Scotia

Site 16, Munich

Site 52, Torino

Site 53, Alicante

Site 18, Girona

Site 19, Seville

3015 GD

Site 33, Rotterdam

30-688

Site 47, Krakow

050474

Site 37, Bucharest

Sponsors
All Listed Sponsors
lead

Corcept Therapeutics

INDUSTRY