A Study of BMS-986442 With Nivolumab With or Without Chemotherapy in Solid Tumors and Non-small Cell Lung Cancer

NCT05543629 · Status: TERMINATED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2025-03-18

Study results available
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Summary

The purpose of this study is to evaluate BMS-986442 in combination with nivolumab (with or without chemotherapy) for its antitumor efficacy and benefit to participants.

Conditions

Interventions

BIOLOGICAL

BMS-986442

Specified dose on specified days

BIOLOGICAL

Nivolumab

Specified dose on specified days

DRUG

Docetaxel

Specified dose on specified days

DRUG

Carboplatin

Specified dose on specified days

DRUG

Pemexetred

Specified dose on specified days

DRUG

Paclitaxel

Specified dose on specified days

Sponsors & Collaborators

Principal Investigators

  • Bristol-Myers Squibb · Bristol-Myers Squibb

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-10-04
Primary Completion
2024-09-12
Completion
2024-09-12
FDA Drug
Yes

Countries

  • United States
  • Australia
  • Italy
  • Poland
  • Spain

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05543629 on ClinicalTrials.gov