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Spots Global Cancer Trial Database for A Study to Evaluate the Safety, Effectiveness and Tolerable Dose of BMS-986393 in Novel Combinations in Participants With Relapsed and/or Refractory Multiple Myeloma

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Trial Identification

Brief Title: A Study to Evaluate the Safety, Effectiveness and Tolerable Dose of BMS-986393 in Novel Combinations in Participants With Relapsed and/or Refractory Multiple Myeloma

Official Title: A Phase 1, Multicenter, Open-label Study to Evaluate the Safety and Preliminary Efficacy of BMS-986393 in Novel Combinations in Participants With Relapsed and/or Refractory Multiple Myeloma and Determine the Recommended Dose for Each Add-on Investigational Component

Study ID: NCT06121843

Study Description

Brief Summary: The purpose of this study is to establish a safe and tolerable dose of BMS-986393 in combinations with alnuctamab, mezigdomide, and iberdomide in participants with relapsed and/or refractory multiple myeloma (RRMM).

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Alabama at Birmingham, Birmingham, Alabama, United States

Local Institution - 0002, Phoenix, Arizona, United States

City of Hope Comprehensive Cancer Center, Duarte, California, United States

Local Institution - 0005, Jacksonville, Florida, United States

Northside Hospital, Atlanta, Georgia, United States

Local Institution - 0011, Boston, Massachusetts, United States

Local Institution - 0027, Boston, Massachusetts, United States

Local Institution - 0001, Rochester, Minnesota, United States

Local Institution - 0010, Omaha, Nebraska, United States

Local Institution - 0004, Hackensack, New Jersey, United States

Local Institution - 0007, Buffalo, New York, United States

Laura and Isaac Perlmutter Cancer Center, New York, New York, United States

Columbia University Irving Medical Center, New York, New York, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

Local Institution - 0023, Pittsburgh, Pennsylvania, United States

Local Institution - 0025, Nashville, Tennessee, United States

University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Local Institution - 0013, Calgary, Alberta, Canada

Local Institution - 0024, Toronto, Ontario, Canada

Contact Details

Name: Bristol-Myers Squibb

Affiliation: Bristol-Myers Squibb

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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