Actively Recruiting

Phase 1
Phase 2
Age: 18Years +
All Genders
NCT06988488

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

Led by Celgene · Updated on 2026-02-02

62

Participants Needed

22

Research Sites

86 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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).

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older with relapsed and refractory multiple myeloma treated with 2 to 4 prior therapies (Phase 1) or 1 to 3 prior therapies (Phase 2)
  • Measurable multiple myeloma confirmed by local lab tests
  • Eastern Cooperative Oncology Group performance status of 0 to 1
  • Adherence to contraception requirements
Not Eligible

You will not qualify if you...

  • Prior treatment with mezigdomide
  • Prior treatment with T cell engaging therapies
  • Prior B cell-maturation antigen (BCMA)-targeting therapy except autologous BCMA-targeted CART-cell therapy given more than 6 months before study
  • Other protocol-defined inclusion or exclusion criteria apply

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 22 locations

1

University of Alabama at Birmingham

Birmingham, Alabama, United States, 35294-3300

Actively Recruiting

2

Yale New Haven Hospital-Smilow Cancer Center

New Haven, Connecticut, United States, 06510

Actively Recruiting

3

Hackensack University Medical Center

Hackensack, New Jersey, United States, 07601

Actively Recruiting

4

University of Texas MD Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

5

Arthur J E Child Comprehensive Cancer Centre

Calgary, Alberta, Canada, T2N 5G2

Actively Recruiting

6

Local Institution - 0026

Vancouver, British Columbia, Canada, V5Z 4E6

Not Yet Recruiting

7

Local Institution - 0027

Halifax, Nova Scotia, Canada, B3H 2Y9

Not Yet Recruiting

8

Princess Margaret Cancer Centre

Toronto, Ontario, Canada, M5G 2M9

Actively Recruiting

9

Local Institution - 0030

Suzhou, Jiangsu, China, 215006

Not Yet Recruiting

10

Local Institution - 0031

Shanghai, Shanghai Municipality, China, 200434

Not Yet Recruiting

11

Universitaetsklinikum Carl Gustav Carus Dresden

Dresden, Germany, 01307

Actively Recruiting

12

Universitaetsklinikum Hamburg-Eppendorf

Hamburg, Germany, 20246

Actively Recruiting

13

Universitaetsklinikum Heidelberg

Heidelberg, Germany, 69120

Actively Recruiting

14

Evangelismos General Hospital of Athens

Athens, Attikí, Greece, 106 76

Actively Recruiting

15

Alexandra General Hospital of Athens

Athens, Attikí, Greece, 115 28

Actively Recruiting

16

St. Olavs Hospital

Trondheim, Sør-Trøndelag, Norway, 7030

Actively Recruiting

17

Sykehusapoteket Ull

Oslo, Norway, 0450

Actively Recruiting

18

Hospital Universitario Marqués de Valdecilla

Santander, Cantabria, Spain, 39008

Actively Recruiting

19

Hospital Universitario de Salamanca - Complejo Asistencial Universitario de Salamanca

Salamanca, Spain, 37007

Actively Recruiting

20

University College London Hospital

London, England, United Kingdom, W1T 7HA

Actively Recruiting

21

Royal Marsden Hospital (Sutton)

London, Sutton, United Kingdom, SM2 5PT

Actively Recruiting

22

The Christie NHS Foundation Trust

Manchester, United Kingdom, M20 4BX

Actively Recruiting

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Research Team

B

BMS Clinical Trials Contact Center www.BMSClinicalTrials.com

CONTACT

F

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

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

2

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