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OncoMatch/Clinical Trials/NCT05615636

A Phase II Trial of Mosunetuzumab, Polatuzumab, Tafasitamab, and Lenalidomide in Patients With Relapsed B-cell NHL

Is NCT05615636 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Mosunetuzumab and Polatuzumab vedotin for hodgkin lymphoma.

Phase 2RecruitingM.D. Anderson Cancer CenterNCT05615636Data as of May 2026

Treatment: Mosunetuzumab · Polatuzumab vedotin · Tafasitamab · LenalidomideTo learn if giving mosunetuzumab in combination with polatuzumab vedotin, tafasitamab, and lenalidomide can help to control relapsed/refractory FL and DLBCL.

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Extracted eligibility criteria

Cancer type

Hodgkin Lymphoma

Non-Hodgkin Lymphoma

Biomarker criteria

Required: MS4A1 overexpression (CD20+)

relapsed CD20+ Follicular Lymphoma grade 1-3a

Required: MS4A1 overexpression (CD20+)

relapsed CD20+ diffuse large B-cell lymphoma

Performance status

WHO 0–1

Prior therapy

Min 1 prior line

Must have received: any prior therapy

Evidence of progression or lack of response following at least 1 prior treatment

Cannot have received: antibody-drug conjugate (polatuzumab vedotin)

Prior treatment with polatuzumab vedotin

Cannot have received: CD20-directed bispecific antibody (mosunetuzumab)

Prior treatment with mosunetuzumab or other CD20-directed bispecific antibodies

Cannot have received: antibody-drug conjugate (tafasitamab)

Prior treatment with tafasitamab and/or lenalidomide

Cannot have received: immunomodulatory agent (lenalidomide)

Prior treatment with tafasitamab and/or lenalidomide

Cannot have received: autologous stem cell transplant

Exception: within 100 days prior to first study treatment administration

Autologous SCT within 100 days prior to first study treatment administration

Cannot have received: CAR-T cell therapy

Exception: within 30 days before first study treatment administration

Prior CAR-T therapy within 30 days before first study treatment administration

Cannot have received: allogeneic stem cell transplant

Prior allogeneic SCT

Cannot have received: solid organ transplant

Prior solid organ transplantation

Lab requirements

Blood counts

Hemoglobin ≥ 9.0 g/dL; Absolute neutrophil count ≥ 1.0 x 10^9/L; Platelet count ≥ 75 x 10^9/L

Kidney function

Calculated creatinine clearance ≥30ml/min by Cockcroft-Gault formula

Liver function

Serum bilirubin <1.5x ULN except in patients with Gilbert's syndrome as defined by >80% unconjugated bilirubin who must have a serum bilirubin of <4x ULN; AST (SGOT) and ALT (SGPT) ≤ 3x ULN or <5x ULN if hepatic metastases are present

Adequate hematologic function (unless abnormalities are related to NHL)... Serum bilirubin <1.5x ULN... AST (SGOT) and ALT (SGPT) ≤ 3x ULN or <5x ULN if hepatic metastases are present... Calculated creatinine clearance ≥30ml/min by Cockcroft-Gault formula

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

US trial sites

  • M D Anderson Cancer Center · Houston, Texas

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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