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Radotinib as 3rd or Later Line Therapy in CP-CML — REVITAL  

Chronic Myeloid Leukemia Clinical Trial

Official title:
Radotinib Efficacy and Safety Validation in Chronic Phase Chronic Myeloid Leukemia Patients Who Are Intolerant or Resistant to at Least Two Tyrosine Kinase Inhibitors As a Third or Subsequent Line Therapy

Clinical Trial Summary

The purpose of this study is to determine whether radotinib is effective and safe for patients with chronic myeloid leukemia, chronic phase who are intolerable or resistant to prior 2 or more tyrosine kinase inhibitors.

Clinical Trial Description

The purpose of this study is to determine whether radotinib 400mg bid is effective and safe for patients with chronic myeloid leukemia, chronic phase who are intolerable or resistant to prior 2 or more tyrosine kinase inhibitors. The primary end point is major cytogenetic response by 12 months. ;

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02422719
Study type Interventional
Source Ulsan University Hospital
Contact Hae Kyung Shin, R.N.
Phone +82-52-230-1418
Email gem9771uuh@naver.com
Status Recruiting
Phase Phase 2
Start date April 2015
Completion date March 2019
View Details
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