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A Study of Subcutaneous Nivolumab + Relatlimab Fixed-dose Combination (FDC) in Previously Untreated Metastatic or Unresectable Melanoma (RELATIVITY-127)

NCT05625399 PHASE3 ACTIVE_NOT_RECRUITING

The purpose of this study is to demonstrate that the study drug exposure level of the nivolumab + relatlimab FDC subcutaneous (SC) formulation is not worse than nivolumab + relatlimab FDC intravenous (IV) administration in participants with previously untreated metastatic or unresectable melanoma.

Details

Lead sponsorBristol-Myers Squibb
PhasePHASE3
StatusACTIVE_NOT_RECRUITING
Enrolment579
Start dateMon Mar 06 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionThu Nov 18 2027 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

Italy, Finland, Poland, Belgium, Sweden, United States, France, Austria, Chile, Israel, Norway, Canada, Spain, Brazil, United Kingdom, Germany, Switzerland, Australia, Czechia