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Study identifier: NCT06953960 Synced from ClinicalTrials.gov · July 29, 2026
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A Study to Assess Adverse Events and Change in Disease Activity of Oral Surzetoclax Alone or in Combination With Subcutaneous and/or Oral Antimyeloma Agents in Adult Participants With Multiple Myeloma (MM)

Condition: Multiple Myeloma  ·  Sponsor: AbbVie

PhasePhase 1/Phase 2
Planned participants199
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Multiple myeloma (MM) is a plasma cell disease characterized by the growth of clonal plasma cells in the bone marrow. The purpose of this study is to assess the safety and change in disease activity of surzetoclax in adult participants with relapsed/refractory (R/R) MM. Adverse events and change in disease activity will be assessed. Surzetoclax is an investigational drug being developed for the treatment of R/R MM. In Substudy 1 there will be a dose escalation phase where participants will receive various doses of surzetoclax in combination with daratumumab + dexamethasone, to determine the best dose of surzetoclax. This will be followed by a dose expansion and selection phase where participants will receive 1 of 2 doses of surzetoclax in combination with daratumumab + dexamethasone, or daratumumab + dexamethasone + pomalidomide (only during the expansion phase). In Substudy 2, there will be a dose escalation phase where participants will receive various doses of surzetoclax alone. Approximately 130 adult participants with R/R MM will be enrolled in the study in approximately 40 sites worldwide. In Substudy 1 escalation phase, participants will receive oral surzetoclax tablets in combination with subcutaneous (SC) daratumumab injections + oral dexamethasone tablets and in the expansion phase, will receive oral surzetoclax tablets in combination with SC daratumumab injections + oral dexamethasone tablets or daratumumab injections + oral pomalidomide + oral dexamethasone tabl…

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 (48)

University of Southern California /ID# 272414Los Angeles, California, United StatesRecruiting
Yale University School of Medicine /ID# 272447New Haven, Connecticut, United StatesRecruiting
Dana-Farber Cancer Institute /ID# 271846Boston, Massachusetts, United StatesRecruiting
University of Michigan Health System - Ann Arbor /ID# 271536Ann Arbor, Michigan, United StatesRecruiting
Memorial Sloan Kettering Cancer Center - New York - York Avenue /ID# 271214New York, New York, United StatesRecruiting
University of North Carolina at Chapel Hill /ID# 272454Chapel Hill, North Carolina, United StatesRecruiting
Atrium Health Levine Cancer Institute /ID# 271510Charlotte, North Carolina, United StatesRecruiting
Wake Forest Baptist Health /ID# 271294Winston-Salem, North Carolina, United StatesRecruiting
Oregon Health and Science University /ID# 272282Portland, Oregon, United StatesRecruiting
University of Texas - Southwestern Medical Center /ID# 271914Dallas, Texas, United StatesRecruiting
Northwest Medical Specialties Tacoma /ID# 272506Tacoma, Washington, United StatesRecruiting
Liverpool Hospital /ID# 272002Liverpool, New South Wales, AustraliaRecruiting

+ 36 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06953960