BMS-986449 Alone and in Combination with Nivolumab in Advanced Solid Tumors

What is the Purpose of this Study?

This study will evaluate the safety and side effects of an investigational drug called BMS-986449 in patients with an advanced solid tumor that has grown or come back. The study also aims to determine the dose of BMS-986449 that can be given to patients for treatment of certain types of cancer. BMS-986449 will be given alone, or in combination with another drug called nivolumab. Researchers will examine how the body absorbs and processes BMS-986449, as well as how the participant’s cancer responds to treatment with BMS-986449 alone or in combination with nivolumab. Nivolumab is an immunotherapeutic antibody that is approved for the treatment of certain types of cancer, but its use in combination with BMS-986449 is investigational.


Eligibility

  • * All participants must have a histologically or cytologically confirmed, advanced, unresectable/metastatic, solid malignancy (measurable by Response Evaluation Criteria in Solid Tumors \[RECIST\] v1.1), and have received, be refractory to, ineligible for, or intolerant of existing therapy(ies) known to provide clinical benefit for the condition of the participant.
  • * Part 1A may have a solid malignancy of any histology.
  • * Part 1B is restricted to participants with Non-small cell lung cancer (NSCLC).
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Where can I participate?

Cedars-Sinai Cancer at The Angeles Clinic and Research Institute

More about this Clinical Trial

What is the full name of this clinical trial?

CA1201001: Phase 1/2 Study of BMS-986449 Alone and in Combination with Nivolumab in Participants with Advanced Solid Tumors

Study Details
Disease Type/Condition

Breast, Cervix, Esophagus, Kidney, Larynx, Liver, Lung, Other Digestive Organ, Small Intestine, Stomach, Urinary Bladder

Principal Investigator

Moyers, Justin

Co-Investigators

Cathie T Chung, Inderjit Mehmi, Kristopher Wentzel, Michelle Offner, Omid Hamid, Vi K. Chiu

Age Group

Adult

Phase

I/II

IRB Number

STUDY00002775

ClinicalTrials.gov ID

NCT05888831

Key Eligibility
ClinicalTrials.gov

How do I learn more about this study?
Email
clinicaltrials@cshs.org
Study Detail
Disease Type/Condition

Breast, Cervix, Esophagus, Kidney, Larynx, Liver, Lung, Other Digestive Organ, Small Intestine, Stomach, Urinary Bladder

Principal Investigator

Moyers, Justin

Age Group

Adult

Phase

I/II

IRB Number

CA1201001

ClinicalTrials.gov ID

NCT05888831

Key Eligibility
ClinicalTrials.gov

Contact
Email
clinicaltrials@cshs.org