A Study of the Safety, Efficacy, and Biomarker Response of BMS-986165 in Participants With Moderate to Severe Ulcerative Colitis

PHASE2CompletedINTERVENTIONAL
Enrollment

38

Participants

Timeline

Start Date

March 15, 2021

Primary Completion Date

May 31, 2023

Study Completion Date

November 29, 2023

Conditions
Colitis, Ulcerative
Interventions
DRUG

BMS-986165

Specified Dose on Specified Days

OTHER

Placebo Comparator

Specified Dose on Specified Days

Trial Locations (26)

2010

Local Institution - 0005, Sydney

3142

Local Institution - 0002, Camberwell

10029

Local Institution - 0015, New York

12200

Local Institution - 0003, Berlin

24105

Local Institution - 0006, Kiel

44195

Local Institution - 0013, Cleveland

60005

Local Institution - 0036, Arlington Heights

71105

Local Institution - 0016, Shreveport

73112

Local Institution - 0020, Oklahoma City

74910

Local Institution - 0039, Lubbock

75044

Local Institution - 0032, Garland

76092

Local Institution - 0033, Southlake

92123

Local Institution - 0014, San Diego

27599-7080

Local Institution - 0026, Chapel Hill

T6K4B2

Local Institution - 0007, Edmonton

N6A 5A5

Local Institution - 0025, London

L4L 4Y7

Local Institution - 0008, Vaughan

01307

Local Institution - 0019, Dresden

1081 HZ

Local Institution - 0009, Amsterdam

02-798

Local Institution - 0031, Warsaw

04-501

Local Institution - 0030, Warsaw

85-231

Local Institution - 0029, Bydgoszcz

85-794

Local Institution - 0028, Bydgoszcz

00935

Local Institution - 0011, San Juan

E11 1NR

Local Institution - 0023, London

CB2 0QQ

Local Institution - 0027, Cambridge

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY

NCT04613518 - A Study of the Safety, Efficacy, and Biomarker Response of BMS-986165 in Participants With Moderate to Severe Ulcerative Colitis | Biotech Hunter | Biotech Hunter