A Study of Nivolumab and Ipilimumab and Nivolumab Alone in Combination With Trans-arterial ChemoEmbolization (TACE) in Participants With Intermediate Stage Liver Cancer
Part of paid clinical trials in Coronado, California.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT04340193
- Phase
- PHASE3
- Status
- Completed
Conditions
- Cancer, Hepatocellular
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- nivolumab — DRUGSpecified dose on specified days
- ipilimumab — DRUGSpecified dose on specified days
- TACE — PROCEDURETACE (Trans-arterial ChemoEmbolization)
Study Details
The purpose of this study is to evaluate the safety and tolerability of nivolumab with and without ipilimumab in combination with Trans-arterial ChemoEmbolization (TACE) to TACE alone in participants with intermediate liver cancer.
Key Dates
- Start date
- Sep 14, 2020
- Status verified
- Nov 2024
- Primary completion
- Dec 12, 2023
- Completion
- Dec 12, 2023
Study Design
- Enrollment
- 26 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Nivolumab + Ipilimumab + TACETACE (Trans-arterial ChemoEmbolization)
- Experimental: Nivolumab + TACE
- Active Comparator: TACE
Primary Outcome Measure
Number of Participants With Adverse Events [ Time Frame: From first dose and 30 days after last dose of study therapy (up to approximately 25 months) ]
Locations (5)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Local Institution - 0189 | Coronado | California | 92118 | - |
| Local Institution | Washington D.C. | District of Columbia | 20007 | - |
| Local Institution - 0005 | Louisville | Kentucky | 40202 | - |
| Local Institution - 0059 | Louisville | Kentucky | 40217 | - |
| Local Institution - 0109 | Dallas | Texas | 75203 | - |