drugset / Trial / NCT04810078

A Study of Subcutaneous Nivolumab Versus Intravenous Nivolumab in Participants With Previously Treated Clear Cell Renal Cell Carcinoma That is Advanced or Has Spread

NCT04810078

Phase 3 Active not recruiting 681 enrolled Bristol-Myers Squibb
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the drug levels, efficacy, safety, and tolerability of subcutaneous nivolumab versus intravenous nivolumab in participants with previously treated clear cell renal cell carcinoma that is advanced or has spread. The purpose of this study's substudy is to evaluate drug level biocomparability of subcutaneous nivolumab manufactured using two different manufacturing processes.

Timeline

Start
2021-05-21
Primary completion
2025-07-29
Completion
2027-05-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Nivolumab Monoclonal antibody 3 mg/kg Subcutaneous
Comparator Nivolumab Monoclonal antibody 1200 mg Subcutaneous
Background rHuPH20 Protein / enzyme biologic 20000 iu Subcutaneous