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

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NCT04810078

Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
681actual
Sites
89
Countries
Argentina, Brazil, Chile +14

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2021-05-21actualWhen the study began enrolling
Primary completion2025-07-29actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-05-10estimatedThe whole study's end, after follow-up
First posted2021-03-22actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-10-09actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Clear Cell Renal Cell Carcinoma

Interventions

  • Biological: Nivolumab and rHuPH20 — also filed as BMS-986298
  • Biological: Nivolumab — also filed as Opdivo, BMS-936558

Primary outcomes

what the primary-completion date above is the date OF
Time-averaged serum concentration over 28 days (Cavgd28)
measured Up to 28 days
Trough serum concentration at steady-state (Cminss)
measured Up to 4 months

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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