CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 219 enrolled
Drug / intervention
BMS-986288 +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03994601
NCT03994601Phase 2Completed

A Phase 1/2 First-in-human Study of BMS-986288 Alone and in Combination With Nivolumab in Advanced Malignant Tumors

Bristol-Myers Squibb·interventional·Posted Jun 21, 2019·Updated Jan 20, 2026

In Brief

A Phase 2 clinical trial evaluating BMS-986288, Nivolumab, and 1 other intervention for Advanced Cancer. Completed, enrolled 219 participants across 40 sites in 7 countries.

Detailed Summary

The purpose of this study is to determine whether BMS-986288 both by itself and in combination with Nivolumab is safe and tolerable in the treatment of select advanced solid tumors.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAdvanced Cancer
CountriesArgentina, Canada, Chile, France, Italy, Spain, United States
Collaborators--

Timeline

Phase 2CompletedFinished
2020202120222023202420252026
First PostedJun 21, 2019
Enrollment StartSep 6, 2019
Primary CompletionAug 31, 2024
TodayJul 2, 2026
Enrollment to primary: 5.0 yearsPosted 7.0 years ago

Interventions

BMS-986288drug

Specified dose on specified days

Nivolumabdrug

Specified dose on specified days

Regorafenibdrug

Specified dose on specified days