drugset / Trial / NCT03184870

A Study of BMS-813160 in Combination With Chemotherapy or Nivolumab in Participants With Advanced Solid Tumors

NCT03184870

Phase 1/2 Completed 332 enrolled Bristol-Myers Squibb
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety profile, tolerability, drug levels, drug effects, and preliminary efficacy of BMS-813160 alone or in combination with either chemotherapy or nivolumab or chemotherapy plus nivolumab in participants with metastatic colorectal and pancreatic cancers.

Timeline

Start
2017-08-08
Primary completion
2023-04-06
Completion
2023-06-14

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-813160 Small molecule 150 mg
Subject BMS-813160 Small molecule 300 mg
Subject BMS-813160 Small molecule 600 mg
Subject Gemcitabine Small molecule
Subject Irinotecan Small molecule
Subject Leucovorin Small molecule
Subject Nivolumab Monoclonal antibody
Subject Paclitaxel Small molecule
Subject fluorouracil Small molecule