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.
Treatment: Mosunetuzumab · Ibrutinib · Acalabrutinib · Zanubrutinib · Pirtobrutinib — The 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
Check if I qualifyExtracted 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
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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