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RecruitingNCT05943522

Asciminib RMP Study

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Trial Parameters

ConditionChronic Myeloid Leukemia
SponsorNovartis Pharmaceuticals
Study TypeOBSERVATIONAL
PhaseN/A
Enrollment100
SexALL
Min Age18 Years
Max Age100 Years
Start Date2023-07-19
Completion2025-07-31
Interventions
Asciminib

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Brief Summary

This study is a prospective, open-label, multi-center, non-comparative, observational study to assess safety and effectiveness of Asciminib in the real-world clinical setting in Korean Chronic myeloid leukemia (CML) patients.

Eligibility Criteria

Inclusion criteria 1. Adult patients diagnosed with Ph+ CP-CML and currently receiving or going to receive Scemblix® treatment according to locally approval label 2. Patients who are willing to provide written informed consent prior to study enrollment Exclusion criteria 1. Patients with contraindication according to locally approved label of Scemblix® 2. Patients who receive or are going to receive any investigational medicine during the observation period

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