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Monoclonal Antibodies
relatlimab for Cancer
Phase 1
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
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up approximately 2 years
Awards & highlights
Study Summary
This trial will study how well two drugs work together to treat advanced tumors, and how safe the combination is.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ approximately 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~approximately 2 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Incidence of Adverse Events (AEs)
Incidence of Adverse Events leading to discontinuation
Incidence of Serious Adverse Events (SAEs)
+6 moreSecondary outcome measures
Incidence of Adverese Events (AEs) in the broad SMQ of Anaphylactic Reaction
Incidence of anti-nivolumab antibodies and neutralizing antibodies (if applicable)
Incidence of anti-relatlimab antibodies and neutralizing antibodies (if applicable)
+1 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: nivolumab + relatlimab + rHuPH20Experimental Treatment3 Interventions
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Relatlimab
FDA approved
Hyaluronidase (human recombinant)
FDA approved
Nivolumab
FDA approved
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Who is running the clinical trial?
Bristol-Myers SquibbLead Sponsor
2,634 Previous Clinical Trials
4,126,831 Total Patients Enrolled
Frequently Asked Questions
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