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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)

525 patients around the world
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)
Available in Argentina, United States, Colombia, Brazil, Spain
Bristol-Myers Squibb
12Research sites
525Patients around the world

This study is for people with

Multiple myeloma
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)

Requirements for the patient

From 18 Years
All Gender

Medical requirements

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.
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.

Sites

Instituto Médico de la Fundación Estudios Clínicos - Rosario
Recruiting
Italia 428, Rosario - Santa Fe
Instituto Médico Especializado Alexander Fleming - CABA, Buenos Aires
Recruiting
Av. Crámer 1180, CABA, Buenos Aires
Sanatorio 9 de Julio - Tucumán
Sanatorio 9 de Julio - Tucumán
Recruiting
San Juan 537, San Miguel de Tucumán, CP 4000
Hospital Italiano de Buenos Aires - CABA, Buenos Aires
Recruiting
Juan Domingo Perón 4190, Piso 1, Ciudad Autónoma de Buenos Aires, C1181ACH
Sanatorio Allende (Nueva Córdoba)
Recruiting
Hipolito Yrigoyen 384, Córdoba
Fundação Antônio Prudente - CAPEC - Centro de Apoio à Pesquisa Clínica
Recruiting
R. Prof. Antônio Prudente, 212 - Liberdade, São Paulo - SP, 01509-010
Hospital Mãe de Deus - Porto Alegre
Recruiting
R. José de Alencar, 286 - Menino Deus, Porto Alegre - RS, 90880-481, Brazil
Instituto Americas - COI
Recruiting
Americas Medical City, Av. Jorge Curi, 550 - Bloco A, Sala 347 - Barra da Tijuca, Rio de Janeiro - RJ, 22775-001
Hospital Sao Rafael
Recruiting
Av. São Rafael, 2152 - São Marcos, Salvador - BA, 41253-190
Hospital Pablo Tobón Uribe
Recruiting
CL 78B #69 - 240, Cordoba, Medellín, Robledo, Medellín, Antioquia, Colombia
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