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A Study to Evaluate Efficacy and Safety of Glinib in Newly Diagnosed CML Patients — IDEAL  

Chronic Myeloid Leukemia Clinical Trial

Official title:
A Phase IV Study to Evaluate Efficacy and Safety of Imatinib(Glinib®) 600mg/Day Depending on Early Molecular Response in Newly Diagnosed Patients With Chronic Myeloid Leukemia in Chronic Phase

Clinical Trial Summary

This study is to evaluate efficacy and safety of Imatinib in two groups of patients; all patients should be diagnosed less than 3 months as chronic myeloid leukemia in a chronic phase. The group A, the reference group, will have 10% or less than 10% of the BCR-ABL level after three month dosing and be maintained their dose of 400mg/day. On the other hand, the group B, will have more than 10% and the dose will be increased from 400mg/day to 600mg/day. The superiority of the group B will be proved by evaluating the MMR rate of these two groups after 12 months of administeration of Imatinib.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02204722
Study type Interventional
Source Dong-A ST Co., Ltd.
Contact
Status Terminated
Phase Phase 4
Start date October 13, 2014
Completion date January 9, 2018
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