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Study identifier: NCT07728188 Synced from ClinicalTrials.gov · July 27, 2026
● Not Yet Recruiting

A Study to Evaluate Adverse Events and Change in Disease Activity With Injected Etentamig Plus Oral Pomalidomide Versus Standard Therapies in Adults With Relapsed or Refractory Multiple Myeloma

Condition: Relapsed or Refractory Multiple Myeloma  ·  Sponsor: AbbVie

PhasePhase 3
Planned participants520
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Multiple myeloma (MM) is a plasma cell malignancy characterized by the proliferation of clonal plasma cells in the bone marrow. The disease primarily localizes to the bones and bone marrow, with resultant cytopenias, bone pain, fractures, infections, hypercalcemia, and renal failure. This study aims to evaluate the safety and change in disease activity of etentamig in combination with pomalidomide compared with standard available therapies in participants with relapsed or refractory multiple myeloma who have received 1-3 prior lines of treatment, including lenalidomide. Etentamig is an investigational drug being developed for the treatment of relapsed or refractory multiple myeloma. This is a randomized, open-label study. The study will include a safety run-in portion and a randomized portion. The safety run-in participants will receive etentamig in combination with pomalidomide. The randomized portion of the study participants will receive either etentamig with pomalidomide or Standard Available Therapies (SATs). Approximately 520 participants will be enrolled in the study at approximately 200 sites worldwide. Prior to initiation of the randomized portion of the study, the safety run-in will be conducted in which participants will receive etentamig injections plus oral pomalidomide. Following review of the safety run-in data and per protocol-defined criteria, the study will advance to the randomized portion where participants will be randomized to receive either etentamig …

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

Talk to the study team

ABBVIE CALL CENTER  ·  844-663-3742  ·  abbvieclinicaltrials@abbvie.com

Always discuss trial participation with your own doctor first.

Locations (66)

University of Arizona Cancer Center /ID# 285339Tucson, Arizona, United States
Toi Clinical Research - Whittier /ID# 284462Cerritos, California, United States
University of California Los Angeles /ID# 282444Los Angeles, California, United States
University Of Colorado - Anschutz Medical Campus /ID# 283478Aurora, Colorado, United States
MedStar Georgetown University Hospital /ID# 283734Washington D.C., District of Columbia, United States
Cleveland Clinic Florida /ID# 283692Weston, Florida, United States
Northwest Georgia Oncology Centers /ID# 284769Marietta, Georgia, United States
Rush University Medical Center /ID# 283095Chicago, Illinois, United States
Beth Israel Deaconess Medical Center /ID# 285204Boston, Massachusetts, United States
Cancer And Hematology Centers Of Western Michigan - Grand Rapids /ID# 282591Grand Rapids, Michigan, United States
The Mount Sinai Hospital /ID# 283535New York, New York, United States
Columbia University Medical Center /ID# 283510New York, New York, United States

+ 54 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07728188