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OncoMatch/Clinical Trials/NCT06492837

Study With Mosunetuzumab and Zanubrutinib in R/R Follicular Lymphoma Patients

Is NCT06492837 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Mosunetuzumab in combination with Zanubrutinib for follicular lymphoma.

Phase 2RecruitingFondazione Italiana Linfomi - ETSNCT06492837Data as of Jun 2026Location: Australia · Italy

Treatment: Mosunetuzumab in combination with ZanubrutinibThis is a Phase 2, multicenter study evaluating the efficacy and safety of mosunetuzumab + zanubrutinib (M+Z) used as salvage strategy in patients with R/R FL who have received at least one line of prior systemic therapy.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Mosunetuzumab in combination with Zanubrutinib

Cancer type

Non-Hodgkin Lymphoma

Biomarker criteria

Required: CD20 overexpression (positive by flow cytometry or immunohistochemistry)

cFL (CD20+ by flow cytometry or immunohistochemistry)

Disease stage

Excluded: Stage I, II

Performance status

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

Prior therapy

Max 3 prior lines
Min 1 prior line

Must have received: anti-CD20 antibody — systemic therapy

At least one and up to three lines of systemic therapy containing an anti-CD20 antibody (anti-CD20 alone and/or in combination with radiotherapy is not considered as a line of therapy).

Cannot have received: Bruton's tyrosine kinase inhibitor

Prior exposure to a Bruton's tyrosine kinase (BTK) inhibitor (BTKi).

Cannot have received: anti-CD20xCD3 bispecific antibody

Prior exposure to an anti-CD20xCD3 bispecific antibody (bsAbs).

Cannot have received: allogeneic hematopoietic stem cell transplantation

Prior allogeneic hematopoietic stem cell transplantation.

Cannot have received: CAR-T cell therapy

Exception: within 90 days prior to first therapy administration

Prior treatment with chimeric antigen receptor T-cell (CAR-T) therapy within 90 days prior to first therapy administration.

Lab requirements

Blood counts

ANC > 1.0 x 10^9/L; Platelet count ≥ 75 x 10^9/L; Hemoglobin ≥ 9 g/dL

Kidney function

creatinine clearance ≥ 40 mL/min (Cockcroft-Gault formula, normalized to 1.72 m2)

Liver function

AST and ALT ≤ 2.5 x ULN; Bilirubin ≤1.5 x ULN (unless due to Gilbert's syndrome or non-hepatic origin)

Adequate hematological counts defined as follows: Absolute neutrophil count (ANC) > 1.0 x 10^9/L; Platelet count ≥ 75 x 10^9/L; Hemoglobin ≥ 9 g/dL. Adequate renal function defined as creatinine clearance ≥ 40 mL/min (Cockcroft-Gault formula, normalized to 1.72 m2). Adequate hepatic function per local laboratory reference range as follows: AST and ALT ≤ 2.5 x ULN; Bilirubin ≤1.5 x ULN (unless bilirubin rise is due to Gilbert's syndrome or of non-hepatic origin).

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

Frequently asked questions

Is NCT06492837 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior Bruton's tyrosine kinase inhibitor, anti-CD20xCD3 bispecific antibody, allogeneic hematopoietic stem cell transplantation disqualifies patients from enrollment.

Does this trial require CD20?

Yes, CD20 overexpression 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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