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OncoMatch/Clinical Trials/NCT07208981

Orelabrutinib Combined With Zebetuzumab and Lenalidomide for the Treatment of Newly Diagnosed MZL

Is NCT07208981 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Orelabrutinib and Zebetuzumab for marginal zone lymphoma(mzl).

Phase 2RecruitingThe First Affiliated Hospital with Nanjing Medical UniversityNCT07208981Data as of Jun 2026Location: China

Treatment: Orelabrutinib · Zebetuzumab · Lenalidomide · Bendamustine + RituximabThis is an open-label, multicenter, phase 2, non-randomized study aiming to evaluate the efficacy and safety of orelabrutinib combined with zebetuzumab and lenalidomide or bendamustine combined with rituximab in the treatment of newly diagnosed marginal zone lymphoma (MZL).

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Bendamustine + Rituximab

Targeted therapy

Orelabrutinib

Endocrine / hormonal

Lenalidomide

Other

Zebetuzumab

Cancer type

Non-Hodgkin Lymphoma

Biomarker criteria

Required: MS4A1 overexpression (CD20-positive)

Histopathologically confirmed CD20-positive marginal zone lymphoma

Disease stage

Required: Stage II 2, IIE, III, IV

Performance status

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

Demographics

Ages ≤ 75

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Lab requirements

Blood counts

absolute neutrophil count ≥1.5×10^9/l, platelets ≥75×10^9/l, hemoglobin ≥75g/l; if accompanied by bone marrow involvement, absolute neutrophil count ≥1.0×10^9/l, platelets ≥50×10^9/l, hemoglobin ≥50g/l

Kidney function

serum creatinine ≤ 1.5 times uln; creatinine clearance rate ≥ 60 ml/min

Liver function

total bilirubin ≤ 1.5 times uln, ast or alt ≤ 2 times uln

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

Frequently asked questions

Is NCT07208981 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Does this trial require MS4A1?

Yes, MS4A1 overexpression is a required biomarker for enrollment.

What disease stage is eligible?

Stage II 2 or IIE or III or IV is required.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

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

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