For Healthcare Professionals

Open-label Study Comparing Iberdomide, Daratumumab and Dexamethasone (IberDd) Versus Daratumumab, Bortezomib, and Dexamethasone (DVd) in Participants With Relapsed or Refractory Multiple Myeloma (RRMM)

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About the study

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).
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria


  1. Documented diagnosis of multiple myeloma (MM) and measurable disease.
  2. Received 1 to 2 prior lines of anti-myeloma therapy.
  3. Must have documented disease progression during or after their last anti-myeloma regimen.
  4. Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1 or 2.

EXCLUSION CRITERIA

Exclusion Criteria


  1. Any condition that confounds the ability to interpret data from the study.
  2. Has plasma cell leukemia, Waldenstrom's macroglobulinemia or POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes), or clinically significant amyloidosis.
  3. Known central nervous system involvement with MM.
  4. Prior therapy with iberdomide.
  5. * Other protocol-defined Inclusion/Exclusion criteria apply.


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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall 855-907-3286Email iconEmail Study Center

Study Details


Contition

Multiple Myeloma

Age

18+

Phase

PHASE3

Participants Needed

864

Est. Completion Date

Jun 25, 2032

Treatment Type

INTERVENTIONAL


Sponsor

Celgene

ClinicalTrials.gov NCT Identifier

NCT04975997

Study Number

CC-220-MM-002

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