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A Phase 3, Two-Stage, Randomized, Multicenter, Open-label Study Comparing Iberdomide, Daratumumab and Dexamethasone (IberDd) Versus Daratumumab, Bortezomib, and Dexamethasone (DVd) in Subjects With Relapsed or Refractory Multiple Myeloma (RRMM)


Description

This is a multicenter, two-stage, randomized, controlled, open-label, Phase 3 study comparing the efficacy and safety of iberdomide in combination with dexamethasone and daratumumab (IberDd) versus daratumumab, bortezomib, and dexamethasone (DVd) in participants with relapsed or refractory multiple myeloma (RRMM).This is a multicenter, two-stage, randomized, controlled, open-label, Phase 3 study comparing the efficacy and safety of iberdomide in combination with dexamethasone and daratumumab (IberDd) versus daratumumab, bortezomib, and dexamethasone (DVd) in participants with relapsed or refractory multiple myeloma (RRMM). Approximately 200 patients randomized in stage 1 to one of three iberdomide dose levels of 1, 1.3, or 1.6 mg in combination with daratumumab and dexamethasone (Treatment Arms A1, A2, or A3), or to the DVd comparator arm (Treatment Arm B). In Stage 2 of the study, approximately 664 additional subjects will be randomized 1:1 between 2 treatment arms: * Approximately

Trial Eligibility

Inclusion Criteria * Documented diagnosis of multiple myeloma (MM) and measurable disease. * Received 1 to 2 prior lines of anti-myeloma therapy. * Must have documented disease progression during or after their last anti-myeloma regimen. * Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1 or 2. Exclusion Criteria * Any condition that confounds the ability to interpret data from the study. * Has plasma cell leukemia, Waldenstrom's macroglobulinemia or POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes), or clinically significant amyloidosis. * Known central nervous system involvement with MM. * Prior therapy with iberdomide. * Other protocol-defined Inclusion/Exclusion criteria apply.

Study Info

Organization

Celgene


Primary Outcome

Progression-free Survival (PFS)


Outcome Timeframe Up to approximately 5 years

NCTID NCT04975997

Phases PHASE3

Primary Purpose TREATMENT

Start Date 2022-06-23

Completion Date 2026-03-18

Enrollment Target 864

Interventions

DRUG Dexamethasone

DRUG Daratumumab

DRUG Bortezomib

DRUG Iberdomide

DRUG Iberdomide

DRUG Iberdomide

Locations Recruiting

Local Institution - 035

United States, Arkansas, Hot Springs


Local Institution - 641

United States, California, Cerritos


Local Institution - 683

United States, California, Corona


Los Angeles Cancer Network - Fountain Valley

United States, California, Fountain Valley


USC Norris Comprehensive Cancer Center

United States, California, Los Angeles


Interested in joining this trial?

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