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Brief Title: A Study to Evaluate Alnuctamab in Combination With Mezigdomide in Participants With Relapsed and/or Refractory Multiple Myeloma
Official Title: A Phase 1b/2a, Multicenter, Open-label Study to Determine the Recommended Dose and Schedule, and Evaluate the Safety and Preliminary Efficacy of Alnuctamab in Combination With Mezigdomide in Participants With Relapsed and/or Refractory Multiple Myeloma
Study ID: NCT06163898
Brief Summary: The purpose of this study is to determine the recommended dose and schedule, and evaluate the safety and preliminary efficacy of alnuctamab in combination with mezigdomide in participants with relapsed and/or refractory multiple myeloma.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Local Institution - 0033, Birmingham, Alabama, United States
Local Institution - 0035, New Haven, Connecticut, United States
Local Institution - 0018, New York, New York, United States
Local Institution - 0021, Petah-Tikva, HaMerkaz, Israel
Local Institution - 0030, Ramat Gan, HaMerkaz, Israel
Local Institution - 0020, Jerusalem, , Israel
Name: Bristol-Myers Squibb
Affiliation: Bristol-Myers Squibb
Role: STUDY_DIRECTOR