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A Study to Assess the Adverse Events and Change in Disease Activity in Adult Participants With Relapsed or Refractory Multiple Myeloma Receiving Oral ABBV-453 Tablets

Active, not recruiting · Phase 1 · NCT05308654

Conditions: Relapsed/Refractory Multiple Myeloma

At a glance

Research payments reported, 2025
$338,765
U.S. investigators named
14
Sites paid
17
Planned or actual enrollment
34

About the trial

Sponsor
AbbVie
Tested
ABBV-453 (drug), Dexamethasone (drug), Daratumumab (drug), Lenalidomide (drug)
Dates
Started 2022-05-17; completion 2025-12
Results posted
Not yet

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 toxicity of ABBV-453 in adult participants with relapsed/refractory (R/R) MM. Adverse events and change in disease activity will be assessed. ABBV-453 is an investigational drug being developed for the treatment of R/R MM. Part 1 will be a monotherapy dose escalation phase to determine the best dose of ABBV-453. In Part 2, participants are placed in 1 of 3 groups called treatment arms. Each group receives a different treatment. Approximately 28 to 48 adult participants in Part 1 and 150 to 312 adult participants in Part…

From ClinicalTrials.gov, last updated 2025-08-14. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $338,765 in research payments for this study in 2025 (78 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.