CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 166 enrolled
Drug / intervention
BMS-986178 +5 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/NCT02737475
NCT02737475Phase 2Completed

A Phase 1/2a Study of BMS-986178 Administered Alone or in Combination With Nivolumab and/or Ipilimumab in Subjects With Advanced Solid Tumors

Bristol-Myers Squibb·interventional·Posted Apr 14, 2016·Updated Jan 25, 2022

In Brief

A Phase 2 clinical trial evaluating BMS-986178, Nivolumab, and 4 other interventions for Advanced Cancer. Completed, enrolled 166 participants across 22 sites in 6 countries.

Detailed Summary

The purpose of the study is to determine the safety and tumor-shrinking ability of experimental medication BMS-986178, when given by itself or in combination with Nivolumab and/or Ipilimumab, in participants with solid cancers that are advanced or have spread.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAdvanced Cancer
CountriesCanada, Israel, Italy, Netherlands, Spain, United States
Collaborators--

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedApr 14, 2016
Enrollment StartJun 17, 2016
Primary CompletionNov 2, 2020
TodayJul 2, 2026
Enrollment to primary: 4.4 yearsPosted 10.2 years ago

Interventions

BMS-986178drug

Specified dose on specified days

Nivolumabdrug

Specified dose on specified days

Ipilimumabdrug

Specified dose on specified days

Tetanus vaccinebiological

Specified dose on specified days

DPV-001 vaccinebiological

DPV-001 (UbiLT3 and UbiLT6): Specified dose on specified days

Cyclophosphamidedrug

Specified dose on specified days