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Study identifier: NCT06988488 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study to Determine the Recommended Dose and Schedule, and Evaluate the Safety and Preliminary Efficacy of Mezigdomide in Combination With Elranatamab in Participants With Relapsed and/or Refractory Multiple Myeloma

Condition: Multiple Myeloma  ·  Sponsor: Celgene

PhasePhase 1/Phase 2
Planned participants62
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the preliminary safety and determine the RP2D of mezigdomide in combination with elranatamab in participants with relapsed and refractory multiple myeloma (RRMM).

This description comes directly from the study's public registry record.

Talk to the study team

BMS Clinical Trials Contact Center www.BMSClinicalTrials.com  ·  855-907-3286  ·  Clinical.Trials@bms.com

First line of the email MUST contain NCT # and Site #.

Always discuss trial participation with your own doctor first.

Locations (22)

University of Alabama at BirminghamBirmingham, Alabama, United StatesRecruiting
Yale New Haven Hospital-Smilow Cancer CenterNew Haven, Connecticut, United StatesRecruiting
Hackensack University Medical CenterHackensack, New Jersey, United StatesRecruiting
University of Texas MD Anderson Cancer CenterHouston, Texas, United StatesRecruiting
Arthur J E Child Comprehensive Cancer CentreCalgary, Alberta, CanadaRecruiting
Local Institution - 0026Vancouver, British Columbia, CanadaNot Yet Recruiting
QEII Health Sciences Centre - Victoria General SiteHalifax, Nova Scotia, CanadaRecruiting
Princess Margaret Cancer CentreToronto, Ontario, CanadaRecruiting
Local Institution - 0030Suzhou, Jiangsu, ChinaNot Yet Recruiting
Local Institution - 0031Shanghai, Shanghai Municipality, ChinaNot Yet Recruiting
Universitaetsklinikum Carl Gustav Carus DresdenDresden, GermanyRecruiting
Universitaetsklinikum Hamburg-EppendorfHamburg, GermanyRecruiting

+ 10 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06988488