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Study identifier: NCT07095452 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study to Assess A Change in Disease Activity and Adverse Events of Intravenous Etentamig and Daratumumab (Etentamig+D) Compared to Daratumumab, Lenalidomide, and Dexamethasone (DRd) in Adult Participants With Newly Diagnosed Multiple Myeloma Not Eligible for Transplant

Condition: Multiple Myeloma  ·  Sponsor: AbbVie

PhasePhase 2/Phase 3
Planned participants660
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Multiple myeloma (MM) is a cancer of the blood's plasma cells. The cancer is typically found in the bones and bone marrow (the spongy tissue inside of the bones) and can cause bone pain, fractures, infections, weaker bones, and kidney failure. This is a study to determine the adverse events, change in disease activity, and pharmacokinetics of Etentamig in adult participants with MM. Etentamig is an investigational drug being developed for the treatment of MM. This study is broken into 2 phases; phase 2 with 3 study arms and phase 3 with 2 study arms. Participants in phase 2 will receive 1 of 3 doses of etentamig in combination with daratumumab. Participants in phase 3 will receive etentamig at RP3D in combination with daratumumab, or daratumumab, lenalidomide, and dexamethasone (DRd). Around 660 adult participants with MM will be enrolled at approximately 155 sites worldwide Participants in phase 2 will receive 1 of 3 doses of etentamig as intravenous (IV) infusions, combination with subcutaneous (SC) injections of daratumumab. Participants in phase 3 will receive RP3D doses of etentamig as IV infusions, combination with SC injections of daratumumab, or SC injections of daratumumab, capsules of lenalidomide, and tablet/ IV injections of dexamethasone (DRd). The study duration is approximately 16 years. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospita…

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 (49)

Mayo Clinic Hospital Scottsdale /ID# 278349Scottsdale, Arizona, United StatesRecruiting
Cedars-Sinai Medical Center /ID# 278238Los Angeles, California, United StatesRecruiting
Colorado Blood Cancer Institute /ID# 279080Denver, Colorado, United StatesRecruiting
Winship Cancer Institute of Emory University /ID# 277667Atlanta, Georgia, United StatesRecruiting
Fort Wayne Medical Oncology And Hematology /ID# 278141Fort Wayne, Indiana, United StatesRecruiting
Minnesota Oncology - Minneapolis Clinic /ID# 278720Minneapolis, Minnesota, United StatesRecruiting
Mayo Clinic Hospital Rochester /ID# 277886Rochester, Minnesota, United StatesRecruiting
Icahn School of Medicine at Mount Sinai /ID# 277844New York, New York, United StatesRecruiting
Memorial Sloan Kettering Cancer Center - New York - York Avenue /ID# 277946New York, New York, United StatesRecruiting
Weill Cornell Medicine Myeloma Center /ID# 278216New York, New York, United StatesRecruiting
University of North Carolina at Chapel Hill /ID# 277708Chapel Hill, North Carolina, United StatesRecruiting
Willamette Valley Cancer Institute and Research Center /ID# 278721Eugene, Oregon, United StatesRecruiting

+ 37 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07095452