Phase II Study Assessing the Efficacy and Toxicity of Olverembatinib Monotherapy in Patients With Newly Diagnosed Chronic Myeloid Leukemia in Chronic Phase
Part of paid clinical trials in Houston, Texas.
- Sponsor
- M.D. Anderson Cancer Center
- Study ID
- NCT06817720
- Phase
- PHASE2
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- olverembatinib — DRUGGIven by PO
Study Details
To learn if olverembatinib can help to control newly diagnosed CML in the chronic phase.
Key Dates
- Start date
- Oct 13, 2025
- Status verified
- May 2026
- Primary completion
- Mar 7, 2027
- Completion
- Mar 7, 2027
Study Design
- Enrollment
- 50 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment with OlveremebatinibPatients will receive single agent olverembatinib at a dose of 30 mg orally every other day (QOD)
Primary Outcome Measure
Safety and adverse events (AEs [ Time Frame: Through study completion; an average of 1 year ]
Central Contacts
- Fadi Haddad, MD346-234-4135
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| MD Anderson Cancer Center | Houston | Texas | 77030 | Fadi Haddad, MD (PRINCIPAL_INVESTIGATOR) |
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