A Study to Evaluate Mezigdomide in Combination With Carfilzomib and Dexamethasone (MeziKD) Versus Carfilzomib and Dexamethasone (Kd) in Participants With Relapsed or Refractory Multiple Myeloma (SUCCESSOR-2)
Running, not enrolling · Phase 3
Conditions studied: Relapsed or Refractory Multiple Myeloma
In brief
The purpose of the study is to compare Mezigdomide (CC-92480/BMS-986348) with carfilzomib and dexamethasone (MeziKD) against carfilzomib and dexamethasone (Kd) in the treatment of RRMM: SUCCESSOR-2.
Key facts
- Study ID
- NCT05552976
- Run by
- Bristol-Myers Squibb
- People needed
- 606
- Starts
- 2023-01-10
- Expected to finish
- 2029-07-25
- Last updated by the study team
- 2026-04-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Participant has documented diagnosis of multiple myeloma and measurable disease, defined as any of the following:.
- i) Myeloma-protein (M-protein) ≥ 0.5 grams/deciliter (g/dL) by serum protein electrophoresis (sPEP), or.
- ii) M-protein ≥ 200 milligrams (mg)/24-hour urine collection by urine protein electrophoresis (uPEP) or,.
- iii) For participants without measurable disease in sPEP or uPEP: serum free light chain levels > 100 mg/liter (L) (10 mg/dL) involved light chain and an abnormal κ/λ free light chain ratio.
- Participant has received at least one prior line of anti-myeloma therapy. Note: One line can contain several phases (e.g., induction, [with or without] hematopoietic stem cell transplant, (with or without) consolidation, and/or [with or without] maintenance therapy).
- Participant must have received prior treatment with lenalidomide and at least 2 cycles of an anti-CD38 monoclonal antibody (mAb) (participants who were intolerant of an anti-CD38 mAb and received < 2 cycles are still eligible).
- Participant achieved minimal response or better to at least 1 prior anti-myeloma therapy.
- Participant must have documented disease progression during or after their last antimyeloma regimen.
You may not qualify if…
- Participant who has had prior treatment with mezigdomide or carfilzomib.
- Participant has previously received allogeneic stem cell transplant at any time or received autologous stem cell transplant within 12 weeks of initiating study treatment.
- Other protocol-defined Inclusion/Exclusion criteria apply.
Where it is running
- Local Institution - 0289 — Annapolis, Maryland, United States
- Local Institution - 0204 — Boston, Massachusetts, United States
- Local Institution - 0046 — Mobile, Alabama, United States
- Local Institution - 0005 — Cerritos, California, United States
- Local Institution - 0190 — Irvine, California, United States
- Local Institution - 0187 — Los Angeles, California, United States
- Local Institution - 0344 — Santa Rosa, California, United States
- Local Institution - 0339 — Stockton, California, United States
- Local Institution - 0279 — Newark, Delaware, United States
- Local Institution - 0341 — Fort Myers, Florida, United States
- Local Institution - 0342 — St. Petersburg, Florida, United States
- Local Institution - 0340 — West Palm Beach, Florida, United States
- Local Institution - 0348 — Atlanta, Georgia, United States
- Local Institution - 0291 — Atlanta, Georgia, United States
- Local Institution - 0346 — Minneapolis, Minnesota, United States
- Local Institution - 0222 — Little Silver, New Jersey, United States
- Local Institution - 0199 — The Bronx, New York, United States
- Local Institution - 0322 — Cleveland, Ohio, United States
- Local Institution - 0172 — Columbus, Ohio, United States
- Local Institution - 0321 — Providence, Rhode Island, United States
- Local Institution - 0338 — Greer, South Carolina, United States
- Local Institution - 0349 — Chattanooga, Tennessee, United States
- Local Institution - 0323 — Nashville, Tennessee, United States
- Local Institution - 0337 — Fort Worth, Texas, United States
- Saint Alphonsus Regional Medical Center — Boise, Idaho, United States
Full record on ClinicalTrials.gov
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