An Investigational Immuno-therapy Study for Safety of Nivolumab in Combination With Ipilimumab to Treat Advanced Cancers
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT02869789
- Phase
- PHASE4
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Nivolumab in combination with Ipilimumab — DRUGSpecified dose on specified days
Study Details
A study to evaluate the safety of Nivolumab given in combination with Ipilimumab in patients with advanced cancers. The initial group will enroll patients with newly diagnosed Stage 4 or non-small cell lung cancer that has come back.
Key Dates
- Start date
- Oct 5, 2016
- Status verified
- Jun 2023
- Primary completion
- May 13, 2022
- Completion
- May 13, 2022
Study Design
- Enrollment
- 1,041 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Nivolumab in combination with IpilimumabSpecified dose on specified days
Primary Outcome Measure
Number of Participants With High Grade (Grade 3-4 and Grade 5) Drug-Related Select Adverse Events (AEs) [ Time Frame: From first dose to 30 days post last dose (Up to approximately 27 months) ]
Locations (61)
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