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Study identifier: NCT06892522 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Recruiting

A Study to Assess Change in Disease Activity and Adverse Events (AE)s in Adult Participants With Multiple Myeloma Receiving T Cell Engaging Bi/Tri-specific Antibodies Intravenously (IV)/Subcutaneously (SC) Alone or in Combinations

Condition: Multiple Myeloma  ·  Sponsor: AbbVie

PhasePhase 1/Phase 2
Planned participants602
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where34 locations · 6 countries

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

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. Treatments are available, but MM can come back (relapsed) or may not get better (refractory) with treatment. This is a study to determine the safety, efficacy, and pharmacokinetics of Etentamig and ABBV-2001 in adult participants with MM. Etentamig and ABBV-2001 are investigational drugs being developed for the treatment of MM. This study is broken into 6 substudies and each substudy consists of a dose escalation phase and dose expansion phase. Participants in substudies 1-4 will receive escalating doses of etentamig alone or with daratumumab and lenalidomide (DR), carfilzomib and dexamethasone (Kd) or lenalidomide (R), followed by etentamig at the dose levels established during the escalation phases alone or with DR, Kd, R. Participants in substudies 1-4 can also receive daratumumab, lenalidomide and dexamethasone (DRd), R, or daratumumab, carfilzomib, and dexamethasone (DKd) as a comparator in the dose expansion phases. Participants in substudies 5-6 will receive escalating doses or at the dose levels established during the escalation phases of ABBV-2001 with iberdomide or mezigdomide. Around 602 adult participants with MM will be enrolled at approximately 75 sites worldwide In substudies 1-3, participants will receive escalating do…

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

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Eastern cooperative oncology group (ECOG) performance of \<= 1. * Confirmed diagnosis of multiple myeloma (MM) according to the International Myeloma Working Group (IMWG) diagnostic criteria with either newly diagnosed or relapsed or refractory (RR) MM, depending on the substudy. Exclusion Criteria: * Participant who has known active central nervous system involvement of MM. * Participant who has known active infection as outlined in the protocol.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (34)

City of Hope National Medical Center /ID# 273132Duarte, California, United StatesRecruiting
City of Hope - Orange County Lennar Foundation Cancer Center /ID# 277911Irvine, California, United StatesRecruiting
Colorado Blood Cancer Institute /ID# 273129Denver, Colorado, United StatesRecruiting
Moffitt Cancer Center /ID# 272628Tampa, Florida, United StatesRecruiting
Winship Cancer Institute of Emory University /ID# 274830Atlanta, Georgia, United StatesRecruiting
Mount Sinai - The Tisch Cancer Institute /ID# 272470New York, New York, United StatesRecruiting
Weill Cornell Medical College /ID# 272517New York, New York, United StatesRecruiting
University of North Carolina at Chapel Hill /ID# 274667Chapel Hill, North Carolina, United StatesRecruiting
Atrium Health Levine Cancer Institute /ID# 276193Charlotte, North Carolina, United StatesRecruiting
Atrium Health Wake Forest Baptist Medical Center /ID# 274847Winston-Salem, North Carolina, United StatesRecruiting
Oncology Hematology Care - Blue Ash /ID# 272918Cincinnati, Ohio, United StatesRecruiting
The Ohio State University /ID# 271336Columbus, Ohio, United StatesRecruiting

+ 22 more locations — full list on the registry record.

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

DuarteIrvineDenverTampa

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