A Study to Evaluate the Safety and Tolerability of BMS-986408 Alone and in Combination With Nivolumab or Nivolumab and Ipilimumab in Participants With Advanced Solid Tumors

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

68

Participants

Timeline

Start Date

August 2, 2022

Primary Completion Date

August 22, 2024

Study Completion Date

July 24, 2025

Conditions
Advanced Solid Tumors
Interventions
DRUG

BMS-986408

Specified dose on specified days

BIOLOGICAL

Nivolumab

Specified dose on specified days

BIOLOGICAL

Ipilimumab

Specified dose on specified days

BIOLOGICAL

Platinum-doublet chemotherapy

Specified dose on specified days

DRUG

Rabeprazole

Specified dose on specified days

Trial Locations (18)

1205

Local Institution - 0020, Geneva

4031

Local Institution - 0012, Basel

9007

Local Institution - 0021, Sankt Gallen

13385

Local Institution - 0018, Marseille

28009

Local Institution - 0025, Madrid

28040

Local Institution - 0022, Madrid

28050

Local Institution - 0023, Madrid

29010

Local Institution - 0024, Málaga

31059

Local Institution - 0019, Toulouse

33076

Local Institution - 0015, Bordeaux

77030

Local Institution - 0003, Houston

94800

Local Institution - 0014, Villejuif

02215

Local Institution - 0010, Boston

07601

Local Institution - 0001, Hackensack

T6G 1Z2

Local Institution - 0007, Edmonton

L8V5C2

Local Institution - 0011, Hamilton

K1H 8L6

Local Institution - 0005, Ottawa

M5G 2M9

Local Institution - 0006, Toronto

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY