A Study of Subcutaneously Injected Epcoritamab Plus Oral Lenalidomide Tablets Compared to Intravenously (IV) Infused Rituximab Plus IV Infused Gemcitabine and IV Infused Oxaliplatin in Adult Participants With Relapsed or Refractory Diffuse Large B-Cell Lymphoma
Part of paid clinical trials in Duarte, California.
- Sponsor
- Genmab
- Study ID
- NCT06508658
- Phase
- PHASE3
- Status
- Active Not Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Epcoritamab — DRUGSubcutaneous Injection
- Rituximab — DRUGIntravenous (IV) Infusion
- Lenalidomide — DRUGOral Capsule
- Oxaliplatin — DRUGIV Infusion
- Gemcitabine — DRUGIV Infusion
Study Details
B-cell Lymphoma is an aggressive and rare cancer of a type of immune cells (a white blood cell responsible for fighting infections). This study will assess how safe and effective epcoritamab plus lenalidomide (E-Len) is compared to rituximab plus gemcitabine and oxaliplatin (R-GemOx) )in treating adult participants with relapsed or refractory (R/R) Diffuse Large B-Cell Lymphoma (DLBCL). Adverse events and change in disease condition will be assessed. Epcoritamab is an investigational drug being developed for the treatment of DLBCL. Study doctors put the participants in 1 of 3 groups, called treatment arms. Each group receives a different treatment. Around 360 adult participants with R/R DLBCL will be enrolled in approximately 165 sites across the world. Participants in arm A will receive subcutaneous (SC) injections of epcoritamab plus oral lenalidomide capsules (E-Len) for up to 12 cycles (each cycle is 28 days). Participants in arm B will receive intravenously (IV) infused R-GemOx for up to 4 cycles (each cycle is 28 days). Participants in arm C will receive SC injections of epcoritamab for up to 12 cycles (each cycle is 28 days). There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.
Key Dates
- Start date
- Aug 13, 2024
- Status verified
- Apr 2026
- Primary completion
- Mar 31, 2028
- Completion
- Mar 31, 2028
Study Design
- Enrollment
- 379 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Arm A: Epcoritamab Plus Lenalidomide (E-Len)Participants will receive E-Len for up to 12 cycles (each cycle is 28 days).
- Experimental: Arm B: Rituximab Plus Gemcitabine and Oxaliplatin (R-GemOx)Participants will receive R-GemOx for up to 4 cycles (each cycle is 28 days)
- Experimental: Arm C: EpcoritamabParticipants will receive epcoritamab for up to 12 cycles (each cycle is 28 days).
Primary Outcome Measure
Arm A vs Arm B: Progression-Free Survival (PFS) [ Time Frame: Up to 4 Years ]
Locations (19)
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