Randomized Evaluation of Radotinib Versus Imatinib in Phase III Study for Efficacy With Chinese Patients (RERISE China)

Patients randomized to the radotinib arms will receive 300 mg of radotinib BID at approximately 12-hour intervals. Patients randomized to the imatinib 400 mg arm will receive imatinib once a day throughout the study.

The primary efficacy endpoint is the rate of Major Molecular Response(MMR) at 12 months (1 month = 4 weeks = 28 days), defined as BCR ABL1/ABL% ≤ 0.1% by international scale. The Molecular Response(MR) rate will be measured every 3 months by Real-time Quantitative(RQ)-Polymerase Chain Reaction(PCR) in a central laboratory. All patients will be treated and/or followed for 12 months (48 weeks) after randomization.

Inclusion criteria

• China who are 18 years of age or older.
• Eastern cooperative oncology group (ECOG) score 0, 1, or 2.
• Patients with confirmed diagnosis of CML-CP within last 6 months.
• Patients with cytogenetically confirmed Ph+ CML in chronic phase
• Patients with typical BCR-ABL1 transcript type such as b2a2 and b3a2.
• Patients with adequate organ function.
• Women of childbearing potential should have negative serum or urine pregnancy test within 14 days before study entry.
• Patients providing written informed consent before initiation of any study-related activities.

Exclusion criteria

• Patients with Philadelphia chromosome negative but BCR-ABL1 positive CML.
• Patients who had been treated with interferon or other targeted anti-cancer therapy which inhibits the growth of leukemic cells
• Concurrently clinically significant primary malignancy
• Patients who previously received radiotherapy
• Patients with impaired cardiac function.
• uncontrolled chronic medical condition