drugset / Trial / NCT02714218

A Study of Two Different Dose Combinations of Nivolumab in Combination With Ipilimumab in Subjects With Previously Untreated, Unresectable or Metastatic Melanoma

NCT02714218 ↗

Phase 3 Completed 387 enrolled Bristol-Myers Squibb
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate two different dose combinations of nivolumab and ipilimumab in the treatment of melanoma.

Timeline

Start
2016-04-04
Primary completion
2017-04-20
Completion
2021-05-28

Outcome

Results reported · no primary-endpoint met/missed verdict (typical of a dose-finding / safety study)

registry p = 0.0144; Odds Ratio (OR) 0.59 (95% CI 0.38 to 0.90) NCT02714218 ↗

paper CONCLUSION: The CheckMate 511 study met its primary end point, demonstrating a significantly lower incidence of treatment-related grade 3-5 AEs with NIVO3+IPI1 versus NIVO1+IPI3. PMID 30811280 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ipilimumab Monoclonal antibody 1 mg/kg Intravenous
Subject Ipilimumab Monoclonal antibody 3 mg/kg Intravenous
Subject Nivolumab Monoclonal antibody 1 mg/kg Intravenous
Subject Nivolumab Monoclonal antibody 3 mg/kg Intravenous
Subject Nivolumab Monoclonal antibody 6 mg/kg Intravenous

Indications