drugset / Trial / NCT03980314

A Study to Compare Nivolumab Drug Product Process D to Nivolumab Drug Product Process C in Participants With Stage IIIa/b/c/d or Stage IV Melanoma After Complete Resection

NCT03980314 ↗

Phase 1 Completed 261 enrolled Bristol-Myers Squibb
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to compare the drug levels, immunogenicity and safety of Nivolumab Process D to Nivolumab Process C after complete resection of stage IIIa/b/c/d or stage IV melanoma.

Timeline

Start
2019-06-24
Primary completion
2021-03-04
Completion
2023-11-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody — —

Indications