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OncoMatch/Clinical Trials/NCT06415708

Obinutuzumab Combined With Bendamustine in the Treatment of Mature B-cell Lymphoma

Is NCT06415708 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Obinutuzumab Combined With Bendamustine for b cell lymphoma.

Phase 2RecruitingInstitute of Hematology & Blood Diseases Hospital, ChinaNCT06415708Data as of Jun 2026Location: China

Treatment: Obinutuzumab Combined With BendamustineThis is a prospective, single-center, single-arm clinical study to evaluate the efficacy and safety of maintenance therapy with obinutuzumab for 2 years in patients ≥ 18 years of age with newly diagnosed mature B-cell lymphoma (including follicular lymphoma\[FL\], marginal zone cell lymphoma\[MZL\] , waldenström macroglobulinemia\[WM\], hairy-cell leukemia variant\[HCL-v\]) who achieved ≥ PR after 6 cycles of obinutuzumab in combination with bendamustine.

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Extracted eligibility criteria

Treatments studied

Other

Obinutuzumab Combined With Bendamustine

Cancer type

Non-Hodgkin Lymphoma

Biomarker criteria

Required: CD20 positivity

histological documentation of CD20 positivity

Performance status

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

Prior therapy

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

Cannot have received: chemotherapy

Mature B-cell lymphoma previously treated with chemotherapy, immunotherapy, or radiation therapy

Cannot have received: immunotherapy

Mature B-cell lymphoma previously treated with chemotherapy, immunotherapy, or radiation therapy

Cannot have received: radiation therapy

Mature B-cell lymphoma previously treated with chemotherapy, immunotherapy, or radiation therapy

Lab requirements

Blood counts

hemoglobin ≥ 7 g/dL; absolute neutrophil count ≥ 1.0 × 10^9/L; platelet count ≥ 50 × 10^9/L

Kidney function

creatinine clearance ≥ 30 mL/min

Liver function

AST or ALT ≤ 2.5 x ULN; Serum bilirubin ≤ 2 x ULN (≤ 3 x ULN for patients with Gilbert's syndrome)

Adequate blood function ... hemoglobin ≥ 7 g/dL absolute neutrophil count ≥ 1.0 × 10^9/L platelet count ≥ 50 × 10^9/L; Normal laboratory values: creatinine clearance ≥ 30 mL/min AST or ALT ≤ 2.5 x ULN Serum bilirubin ≤ 2 x ULN (≤ 3 x ULN for patients with Gilbert's syndrome)

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

Frequently asked questions

Is NCT06415708 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 CD20?

Yes, CD20 positivity is a required biomarker for enrollment.

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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