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Immunotherapy
Nivolumab + BMS-986205 for Melanoma
Phase 3
Waitlist Available
Research Sponsored by Bristol-Myers Squibb
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from first dose to 30 days following last dose (up to approximately 25 months)
Awards & highlights
Study Summary
The purpose of this study is to see if BMS-986205 combined with nivolumab, compared to nivolumab by itself, is more effective in treating Melanoma that has spread or is unable to be removed by surgery, and has not previously been treated
Eligible Conditions
- Melanoma
- Skin Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from first dose to 30 days following last dose (up to approximately 25 months)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from first dose to 30 days following last dose (up to approximately 25 months)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Number of Participants Experiencing Adverse Events
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Nivolumab + BMS-986205Experimental Treatment2 Interventions
Specified dose on specified day.
Participants have the option to discontinue BMS-986205, and continue nivolumab monotherapy, at investigator discretion
Group II: Nivolumab + PlaceboActive Control2 Interventions
Specified dose on specified day
Participants will no longer receive BMS-986205 Placebo
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Linrodostat
Not yet FDA approved
Nivolumab
FDA approved
Find a Location
Who is running the clinical trial?
Bristol-Myers SquibbLead Sponsor
2,646 Previous Clinical Trials
4,131,123 Total Patients Enrolled
177 Trials studying Melanoma
57,465 Patients Enrolled for Melanoma
Frequently Asked Questions
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