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NCT06950034
A Phase 1 Study of STX-0712 in Patients With Advanced Hematological Malignancies (CMML and AML)
This is a first-in-human, multicenter, open-label, phase 1 study to evaluate the safety, PK, PD and preliminary efficacy of STX-0712 in patients with advanced CMML and AML for whom there are no further treatment options known to confer clinical benefit.
Trial Details
NCT ID NCT06950034
Phase PHASE1
Sponsor Solu Therapeutics, Inc
Status RECRUITING
Cancer Type Leukemia
Interventions
Locations (sample) Stanford, California, United States|37.42411,-122.16608 Tampa, Florida, United States|27.94752,-82.45843 Boston, Massachusetts, United States|42.35843,-71.05977 Rochester, Minnesota, United States|44.02163,-92.4699 Portland, Oregon, United States|45.52345,-122.67621
Key Eligibility Criteria
Refractory/resistant CMML, defined as: Diagnosis of CMML 1 or 2; and has not responded to at least 4 cycles of hypomethylating agents (HMAs)(for my… Relapsed/refractory monocytic or monocytic predominant AML. Monocytic predominant AML is defined as ≥50% monocytes and/or monocytic precursors (pro… Eastern Cooperative Oncology Group (ECOG) Performance Status ≤2. Life expectancy of \>2 months and stable enough to complete two cycles of STX-0712, in the opinion of the Investigator.
For full eligibility, visit ClinicalTrials.gov .
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