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NCT06508658ACTIVE_NOT_RECRUITINGanonymous

A Phase 3, Multicenter, Randomized, Open-Label Study of Epcoritamab Plus Lenalidomide Compared to Rituximab Plus Gemcitabine and Oxaliplatin in Participants With Relapsed or Refractory Diffuse Large B-Cell Lymphoma

Sponsor

Source record

Genmab

Phase

Source record

PHASE3

Modality

AI-normalized

monoclonal antibody

Target

AI-normalized

Epcoritamab, Rituximab, Lenalidomide, Oxaliplatin, Gemcitabine

Indication / condition

AI-normalized

Diffuse Large B-Cell Lymphoma

Intervention

Source record

Epcoritamab, Rituximab, Lenalidomide, Oxaliplatin, Gemcitabine

Source & freshness

Source record

NCT ID

NCT06508658

Original source

ClinicalTrials.gov

Source last updated

Apr 08, 2026

Ingested at

Jun 11, 2026

Internal sync

Jun 11, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT06508658

Title

A Phase 3, Multicenter, Randomized, Open-Label Study of Epcoritamab Plus Lenalidomide Compared to Rituximab Plus Gemcitabine and Oxaliplatin in Participants With Relapsed or Refractory Diffuse Large B-Cell Lymphoma

Sponsor

Genmab

Status

ACTIVE_NOT_RECRUITING

Phase

PHASE3

Condition raw

Diffuse Large B-Cell Lymphoma

Condition normalized

Diffuse Large B-Cell Lymphoma

Modality raw

monoclonal antibody

Modality normalized

monoclonal antibody

Target raw

Epcoritamab, Rituximab, Lenalidomide, Oxaliplatin, Gemcitabine

Target normalized

Epcoritamab, Rituximab, Lenalidomide, Oxaliplatin, Gemcitabine

Interventions

Epcoritamab, Rituximab, Lenalidomide, Oxaliplatin, Gemcitabine

Public preview

Source record

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.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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