Radotinib Versus Imatinib in Newly Diagnosed Philadelphia Chromosome and Chronic Myeloid Leukemia Chronic Phase Patients

• Status: Completed
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

In this study, the efficacy and safety of two radotinib doses, 300 mg twice daily and 400 mg twice daily, will be compared with imatinib 400 mg once daily in newly diagnosed patients with Philadelphia chromosome-positive (Ph+) Chronic Myelogenous Leukemia in the chronic phase (CML-CP).

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Il-Yang Pharm. Co., Ltd.
• Treatments: Imatinib Mesylate

Criteria

Inclusion Criteria:

• Patients with confirmed diagnosis of chronic phase CML within last 3 months

• Patients with cytogenetically confirmed Ph positive CML in early chronic phase

Exclusion Criteria:

• Patients with Philadelphia chromosome negative but BCR-ABL positive CML

• Patients who used imatinib for 8 days or longer before study entry

• Patients who had been treated with other targeted anti-cancer therapy, except for Hydrea or Agrylin, which inhibits the growth of leukemic cells

• Patients with impaired cardiac function

• Cytologically confirmed CNS involvement

• Severe or uncontrolled chronic medical condition

• Other significant congenital or acquired bleeding disorders that are not related to underlying leukemia

• Patients who had a major surgery within 4 weeks prior to study entry or has not recovered from side effects of such surgery