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 — DRUG
    GIven 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 Olveremebatinib
    Patients 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

Locations (1)

FacilityCityStateZIPSite coordinators
MD Anderson Cancer CenterHoustonTexas77030
Fadi Haddad, MD
346-234-4135
Fadi Haddad, MD (PRINCIPAL_INVESTIGATOR)

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