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OncoMatch/Clinical Trials/NCT05846750

Obinutuzumab in Combination With Lenalidomide in Relapsed or Refractory Marginal Zone Lymphoma

Is NCT05846750 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Obinutuzumab and lenalidomide for marginal zone lymphoma.

Phase 2RecruitingInstitute of Hematology & Blood Diseases Hospital, ChinaNCT05846750Data as of Jun 2026Location: China

Treatment: Obinutuzumab · lenalidomideThis is a prospective, multicenter clinical study that will enroll 59 patients with relapsed and refractory (R/R) MZL. The study is designed to evaluate the efficacy and safety of the combination of obinutuzumab and lenalidomide in the treatment of relapsed and refractory marginal zone lymphoma (MZL).

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Obinutuzumab

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: systemic lymphoma therapy

Prior treatment with at least one line of systemic lymphoma including prior immunotherapy or chemoimmunotherapy

Cannot have received: lenalidomide (lenalidomide)

Exception: not refractory or resistant

Patients who are refractory or resistant to lenalidomide

Cannot have received: obinutuzumab (obinutuzumab)

Exception: not refractory or resistant

Patients who are refractory or resistant to obinutuzumab

Cannot have received: thalidomide (thalidomide)

Previous ≥ Grade 3 allergic reactions/Hypersensitivity to thalidomide

Lab requirements

Blood counts

Hemoglobin ≥ 7 g/dL; Absolute neutrophil count ≥ 1.0 × 10^9/L; Platelet count ≥ 50 x 10^9/L

Kidney function

Creatinine clearance ≥ 30 mL/min

Liver function

Glutathione transaminase(AST) or glutathione aminotransferase (ALT) ≤ 2.5 x upper limit of normal (ULN); Serum bilirubin ≤ 2 × ULN (≤ 3 × ULN in patients with Gilbert's syndrome)

Adequate blood function... Hemoglobin ≥ 7 g/dL; Absolute neutrophil count ≥ 1.0 × 10^9/L; Platelet count ≥ 50 x 10^9/L; Creatinine clearance ≥ 30 mL/min; Glutathione transaminase(AST) or glutathione aminotransferase (ALT) ≤ 2.5 x upper limit of normal (ULN); Serum bilirubin ≤ 2 × ULN (≤ 3 × ULN in patients with Gilbert's syndrome)

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

Frequently asked questions

Is NCT05846750 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior lenalidomide, obinutuzumab, thalidomide 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.

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