OncoMatch

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 (Jun 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 Jun 2026Location: China

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

Check if I qualify

Extracted eligibility criteria

Treatments studied

Immunotherapy

RituximabRituximab

Targeted therapy

Orelabrutinib

Endocrine / hormonal

Lenalidomide

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.

Frequently asked questions

Is NCT06082102 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior BTK inhibitor, lenalidomide plus rituximab (R2 regimen) disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify