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A Study of Subcutaneous Nivolumab + Relatlimab Fixed-dose Combination (FDC) in Previously Untreated Metastatic or Unresectable Melanoma (RELATIVITY-127)
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 sponsor | Bristol-Myers Squibb |
|---|---|
| Phase | PHASE3 |
| Status | ACTIVE_NOT_RECRUITING |
| Enrolment | 579 |
| Start date | Mon Mar 06 2023 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Thu Nov 18 2027 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Melanoma
Interventions
- Nivolumab + Relatlimab
- rHuPH20
Countries
Italy, Finland, Poland, Belgium, Sweden, United States, France, Austria, Chile, Israel, Norway, Canada, Spain, Brazil, United Kingdom, Germany, Switzerland, Australia, Czechia