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OncoMatch/Clinical Trials/NCT07052695

Mosunetuzumab for CLL MRD Clearance

Is NCT07052695 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies multiple treatments for leukemia.

Phase 1/2RecruitingInhye AhnNCT07052695Data as of May 2026

Treatment: Mosunetuzumab · Ibrutinib · Acalabrutinib · Zanubrutinib · PirtobrutinibThe goal of this study is to test mosunetuzumab given alone or in combination with a Bruton tyrosine kinase inhibitor (BTKi, such as ibrutinib, acalabrutinib, zanubrutinib, or pirtobrutinib) in participants with CLL (chronic lymphocytic leukemia) or small lymphocytic lymphoma (SLL). The names of the study drugs in this research study are: * Mosunetuzumab * BTK inhibitor: Ibrutinib, acalabrutinib, zanubrutinib, or pirtobrutinib

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Extracted eligibility criteria

Cancer type

Acute Myeloid Leukemia

Acute Lymphoblastic Leukemia

Chronic Lymphocytic Leukemia

Non-Hodgkin Lymphoma

Performance status

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

Prior therapy

Max 2 prior lines
Min 1 prior line

Must have received: BTK inhibitor (ibrutinib, acalabrutinib, zanubrutinib, pirtobrutinib) — first- or second-line

On continuous BTKi therapy for > 12 months, including > 2 months at a stable dose. The BTKi is the first- or second-line therapy for CLL.

Must have received: BCL2 inhibitor (venetoclax) — first- or second-line

Completed BCL2i-based therapy < 12 months of enrollment. BCL2i-based therapy must be the most recent CLL therapy prior to enrollment. BCL2i must have been given for at least 6 months for patients who were intolerant to a BCL2i and stopped the treatment without disease progression. For all others, at least 12 cycles of BCL2i therapy are required. BCL2i-based regimens include venetoclax plus obinutuzumab (VO) or rituximab (VR), and the combination of a BTKi + a BCL2i +/- anti-CD20mAb.

Cannot have received: CAR-T cell therapy

Exception: within 30 days of starting study therapy

Prior treatment with chimeric antigen receptor T-cell therapy within 30 days of starting study therapy

Cannot have received: radioimmunotherapy

Exception: within 12 weeks of starting study therapy

radioimmunotherapy within 12 weeks of starting study therapy

Lab requirements

Blood counts

Adequate organ and bone marrow function as defined by the study protocol.

Kidney function

Adequate organ and bone marrow function as defined by the study protocol.

Liver function

Adequate organ and bone marrow function as defined by the study protocol.

Adequate organ and bone marrow function as defined by the study protocol.

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

US trial sites

  • Brigham & Women's Hospital · Boston, Massachusetts
  • Dana-Farber Cancer Institute · Boston, Massachusetts

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