A Study to Assess BMS-986453 in Participants With Relapsed and/or Refractory Multiple Myeloma

ID#: NCT06153251

Age: 18 years - 66+

Gender: All

Healthy Subjects: No

Study Phase: Phase 1

Recruitment Status: Recruiting

Start Date: January 23, 2024

End Date: May 02, 2030

Contact Information:
BMS Clinical Trials Contact Center www.BMSClinicalTrials.com
855-907-3286
First line of the email MUST contain NCT # and Site #.
Summary: The purpose of this study is to assess BMS-986453 in participants with relapsed and/or refractory multiple myeloma (RRMM).
Eligibility:

Inclusion Criteria:

- Participants must have a diagnosis of multiple myeloma with relapsed and/or refractory disease.

- Participants must have confirmed progressive disease on or within 12 months (measured from the last dose) of completing treatment with the last anti-myeloma treatment regimen before study entry.

- Participants in Part A and Part B Cohort 1 and in Part B Cohort 2 must have relapsed/refractory multiple myeloma and received previous antimyeloma therapy, including a proteasome inhibitor and an immunomodulatory agent.

- Participants must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

- Participants must have adequate organ function.

Exclusion Criteria:

- Participants must not have any known active or history of central nervous system (CNS) involvement of multiple myeloma.

- Participants must not have active or history of plasma cell leukemia, Waldenstrom's macroglobulinemia, POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, skin changes) syndrome, or clinically significant amyloidosis.

- Participants must not have a history or presence of clinically significant CNS pathology such as seizure disorder, aphasia, stroke, severe brain injury, dementia, Parkinson's disease, or cerebellar disease, or presence of clinically active psychosis.

- Other protocol-defined inclusion/exclusion criteria apply.