Phase II Study Assessing the Safety and Efficacy of Dasatinib in Combination With Ropeginterferon 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
- NCT07269470
- Phase
- PHASE2
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Dasatinib — DRUGGiven orally daily for 3 cycles
- Ropeginterferon alfa-2b (P1101) — DRUGGiven subcutaneous through injection
Study Details
The goal of this clinical research study is to find out if treatment with a combination of dasatinib plus ropeginterferon can help to control CML-CP. The safety of this combination will also be studied.
Key Dates
- Start date
- Nov 1, 2026
- Status verified
- Dec 2025
- Primary completion
- Nov 1, 2029
- Completion
- Nov 1, 2029
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Phase 2 Treatment with Dasatinib (PO) + Ropeginterferon (SC)Participants will receive treatment on an outpatient basis.
Primary Outcome Measure
Safety and Adverse Events (AEs) [ Time Frame: Through study completion; an average of 1 year ]
Central Contacts
- Fadi Haddad, MD713-792-0970
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The University of Texas M. D. Anderson Cancer Center | Houston | Texas | 77030 | Fadi Haddad, MD (PRINCIPAL_INVESTIGATOR) |
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