A Study to Assess Safety of Relatlimab With Ipilimumab in Participants With Advanced Melanoma Who Progressed on Anti-Programmed Cell Death Protein 1 (Anti-PD-1) Treatment

PHASE1TerminatedINTERVENTIONAL
Enrollment

11

Participants

Timeline

Start Date

December 9, 2021

Primary Completion Date

July 26, 2023

Study Completion Date

July 26, 2023

Conditions
Melanoma
Interventions
DRUG

Relatlimab

Specified dose on specified days

DRUG

Ipilimumab

Specified dose on specified days

Trial Locations (28)

1000

Local Institution - 0018, Brussels

1090

Local Institution - 0016, Brussels

1200

Local Institution - 0038, Brussels

2020

Local Institution - 0017, Antwerp

14004

Local Institution - 0030, Córdoba

20014

Local Institution - 0031, Donostia / San Sebastian

23562

Local Institution - 0032, Lübeck

28034

Local Institution - 0029, Madrid

30625

Local Institution - 0035, Hanover

33136

Local Institution - 0015, Miami

35128

Local Institution - 0053, Padua

45147

Local Institution - 0034, Essen

46009

Local Institution - 0028, Valencia

48109

Local Institution - 0003, Ann Arbor

53100

Local Institution - 0055, Siena

60611

Local Institution - 0004, Chicago

69120

Local Institution - 0033, Heidelberg

85724

Local Institution - 0023, Tucson

90033

Local Institution - 0002, Los Angeles

Local Institution - 0005, Los Angeles

90404

Local Institution - 0001, Santa Monica

90419

Local Institution - 0040, Nuremberg

91054

Local Institution - 0037, Erlangen

07960

Local Institution - 0008, Morristown

K1H 8L6

Local Institution - 0044, Ottawa

07548

Local Institution - 0036, Gera

08035

Local Institution - 0026, Barcelona

08908

Local Institution - 0027, Hospitalet de Llobregat - Barcelona

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY

NCT03978611 - A Study to Assess Safety of Relatlimab With Ipilimumab in Participants With Advanced Melanoma Who Progressed on Anti-Programmed Cell Death Protein 1 (Anti-PD-1) Treatment | Biotech Hunter | Biotech Hunter