CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 12 enrolled
Drug / intervention
BMS-986205 +1 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/NCT03792750
NCT03792750Phase 2Completed

A Phase 1/2 Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of BMS-986205 Alone and in Combination With Nivolumab in Chinese Patients With Advanced Malignant Solid Tumors

Bristol-Myers Squibb·interventional·Posted Jan 3, 2019·Updated Feb 28, 2022

In Brief

A Phase 2 clinical trial evaluating BMS-986205 and Nivolumab for Advanced Cancer. Completed, enrolled 12 participants across 1 site.

Detailed Summary

The purpose of this study is to determine safety and effectiveness of experimental medication BMS-986205 in combination with Nivolumab in patients with cancers that are advanced or have spread.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAdvanced Cancer
CountriesChina
Collaborators--

Timeline

Phase 2CompletedFinished
20192020202120222023202420252026
First PostedJan 3, 2019
Enrollment StartDec 31, 2018
Primary CompletionDec 18, 2020
TodayJul 2, 2026
Enrollment to primary: 2.0 yearsPosted 7.5 years ago

Interventions

BMS-986205drug

Specified Dose on Specified Day

Nivolumabbiological

Specified Dose on Specified Day