Purpose of this Study
We are doing this study to find out if an experimental drug called iberdomide (the study drug) is a safe and effective option for multiple myeloma (MM). We also want to what the most appropriate dose and timing for taking the study drug should be.
Who Can Participate?
Eligibility
Adults ages 18+ who:
- Have multiple myeloma that is not responding to therapy; OR
- Have multiple myeloma that has come back after previous therapy
What is Involved?
Description
This study has three periods: a screening period, the study drug period, and a follow-up period.
If you choose to join this study, during the screening period you will:
- Have a physical exam
- Have blood draws
- Give urine samples
- Have imaging tests (X-Ray, MRI/CT/PET scans)
- Have a bone marrow biopsy
- Group A1: you will take a regimen of 1 mg of the study drug along with the drugs daratumumab and dexamethasone
- Group A2: you will take a regimen of 1.3 mg of the study drug along with the drugs daratumumab and dexamethasone
- Group A3: you will take a regimen of 1.6 mg of the study drug along with the drugs daratumumab and dexamethasone
- Group B: you will take a regimen of bortezomib, daratumumab, and dexamethasone (standard MM treatment)
- Group A: you will take a regimen of the study drug along with the drugs daratumumab and dexamethasone
- Group B: you will take a regimen of bortezomib, daratumumab, and dexamethasone
Study Details
Full Title
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)
Principal Investigator
Cristina
Gasparetto
Protocol Number
PRO00111593
NCT ID
NCT04975997
Phase
III
Enrollment Status
Open to Enrollment