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