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OncoMatch/Clinical Trials/NCT06082102

Efficacy and Safety of Orelabrutinib Combined With Rituximab Versus Lenalidomide Combined With Rituximab in Patients With Relapsed/Refractory Marginal Zone Lymphoma

Is NCT06082102 recruiting? Yes, currently enrolling (May 2026). This Phase 3 trial studies multiple treatments including Orelabrutinib and Rituximab for relapsed/refractory marginal zone lymphoma.

Phase 3RecruitingBeijing InnoCare Pharma Tech Co., Ltd.NCT06082102Data as of May 2026

Treatment: Orelabrutinib · Rituximab · Lenalidomide · RituximabEfficacy and Safety of Orelabrutinib Combined with Rituximab versus Lenalidomide Combined with Rituximab in Patients with Relapsed/Refractory Marginal Zone Lymphoma

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Extracted eligibility criteria

Cancer type

Non-Hodgkin Lymphoma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 1 prior line

Must have received: anti-CD20 monoclonal antibody-containing regimen

Prior systemic therapy including at least one anti-CD20 monoclonal antibody-containing regimen is required, with the following specifications: For combination therapies: Minimum of 2 completed treatment cycles For anti-CD20 monotherapy: Minimum of 4 administered doses Progression during treatment waives cycle/dose requirements

Cannot have received: BTK inhibitor

Prior treatment with any types of BTK inhibitor

Cannot have received: lenalidomide plus rituximab (R2 regimen) (lenalidomide, rituximab)

Exception: Patients refractory to lenalidomide plus rituximab (R2 regimen). Refractoriness is defined as either: Failure to achieve at least partial response (PR) after completing an adequate R2 treatment course (≥2 cycles at standard doses), OR Disease progression during R2 therapy or within 6 months after the last dose.

Patients refractory to lenalidomide plus rituximab (R2 regimen). Refractoriness is defined as either: Failure to achieve at least partial response (PR) after completing an adequate R2 treatment course (≥2 cycles at standard doses), OR Disease progression during R2 therapy or within 6 months after the last dose.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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