A Study to Evaluate Whether Participants With Melanoma Prefer Subcutaneous vs Intravenous Administration of Nivolumab and Nivolumab + Relatlimab Fixed-dose Combinations

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

November 6, 2023

Primary Completion Date

April 10, 2025

Study Completion Date

August 31, 2027

Conditions
Melanoma
Interventions
DRUG

relatlimab+nivolumab

Specified dose on specified days

DRUG

relatlimab+nivolumab+rHuPH20

Specified dose on specified days

DRUG

nivolumab

Specified dose on specified days

DRUG

nivolumab+rHuPH20

Specified dose on specified days

Trial Locations (31)

10002

Local Institution - 0003, San Pedro Alcántara, Málaga

10126

Local Institution - 0004, Torino

20141

Local Institution - 0018, Milan

24127

Local Institution - 0017, Bergamo

30120

Local Institution - 0009, Cartagena

30342

Local Institution - 0034, Atlanta

35128

Local Institution - 0012, Padua

39008

Local Institution - 0027, Cantabria

41013

Local Institution - 0006, Seville

41017

Local Institution - 0032, Edgewood

47014

Local Institution - 0035, Meldola

80131

Local Institution - 0026, Napoli

87106

Local Institution - 0028, Albuquerque

98026

Local Institution - 0036, Issaquah

98104

Local Institution - 0030, Seattle

4070196

Local Institution - 0005, Concepción

8331010

Local Institution - 0015, Las Condes

99508-2974

Local Institution - 0007, Anchorage

85054-4502

Local Institution - 0013, Phoenix

94115-3010

Local Institution - 0010, San Francisco

98026-8032

Local Institution - 0037, Edmonds

546 22

Local Institution - 0019, Thessaloniki

115 27

Local Institution - 0014, Athens

151 25

Local Institution - 0029, Marousi

155 62

Local Institution - 0023, Holargos, Athens

185 47

Local Institution - 0008, Piraeus

564 29

Local Institution - 0033, Thessaloniki

00144

Local Institution - 0021, Roma

08025

Local Institution - 0011, Barcelona

08908

Local Institution - 0022, Barcelona

08916

Local Institution - 0020, Badalona

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY

NCT06101134 - A Study to Evaluate Whether Participants With Melanoma Prefer Subcutaneous vs Intravenous Administration of Nivolumab and Nivolumab + Relatlimab Fixed-dose Combinations | Biotech Hunter | Biotech Hunter