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RecruitingLast updated:15 August 2023

RELATIVITY-127: This study is comparing the safety and effectiveness of different ways of administering combination immunotherapy in people with previously untreated metastatic or inoperable melanomaA Phase 3, Randomized, Open-label, Study of Subcutaneous Nivolumab + Relatlimab Fixed-dose Combination Versus Intravenous Nivolumab + Relatlimab Fixed-dose Combination in Participants With Previously Untreated Metastatic or Unresectable Melanoma

Clinical summary

Summary

Eligible participants will be randomly allocated to one of two treatment arms. In Arm A (Experimental), participants will receive a fixed dose combination of nivolumab + relatlimab immunotherapy which will be administered via a subcutaneous injection. In Arm B (Active Comparator), participants will receive a fixed dose combination of nivolumab + relatlimab immunotherapy which will be administered via IV.

Age

People12+

Phase

III

Trial Acronym

RELATIVITY-127

More information

Trial Identifiers

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Commercial Sponsor

Bristol-Myers Squibb (BMS)

Scientific Title

A Phase 3, Randomized, Open-label, Study of Subcutaneous Nivolumab + Relatlimab Fixed-dose Combination Versus Intravenous Nivolumab + Relatlimab Fixed-dose Combination in Participants With Previously Untreated Metastatic or Unresectable Melanoma

Eligibility

Inclusion

  • You have certain types of non-cancer medical conditions.
  • You have been diagnosed with a prior or secondary type of cancer.
  • You have had certain treatments, surgical procedures or drugs.

Exclusion

  • You have been diagnosed with cancer, but have not received any treatment.
  • Your cancer has not spread to other parts of the body.
  • Your cancer has spread to other parts of the body.
Message

Clinical trials have complex eligibility criteria.

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