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Clinical Trial Summary

Uncontrolled, central registration system, all-case, multicenter, special drug use-results surveillance.


Clinical Trial Description

The objective of this study is to collect data on the occurrence, severity, clinical courses of the safety specifications of asciminib, identify factors etc. involved in occurrence and assess its clinical safety inresistant/intolerant chronic myelogenous leukemia patients during an observational period of 48 weeks from the start of treatment with asciminib. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05421091
Study type Observational
Source Novartis
Contact
Status Completed
Phase
Start date July 4, 2022
Completion date February 29, 2024

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