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RECRUITING
NCT05943522

Asciminib RMP Study

Sponsor: Novartis Pharmaceuticals

View on ClinicalTrials.gov

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.

Official title: A Post Approval Surveillance of Scemblix® (Asciminib) in Patients With Chronic Myeloid Leukemia (CML) in Korea

Key Details

Gender

All

Age Range

18 Years - 100 Years

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2023-07-19

Completion Date

2025-07-31

Last Updated

2025-01-14

Healthy Volunteers

No

Interventions

OTHER

Asciminib

There is no treatment allocation. Asciminib will be prescribed by the physician as per locally approved label. No drug will be dispensed from Novartis

Locations (14)

Novartis Investigative Site

Wŏnju, Gangwon-do, South Korea

Novartis Investigative Site

Uijeongbu-si, Gyeonggi-do, South Korea

Novartis Investigative Site

Gyeonggi-do, Korea, South Korea

Novartis Investigative Site

Seoul, Seocho Gu, South Korea

Novartis Investigative Site

Incheon, South Korea

Novartis Investigative Site

Jeollanam, South Korea

Novartis Investigative Site

Pusan, South Korea

Novartis Investigative Site

Seoul, South Korea

Novartis Investigative Site

Seoul, South Korea

Novartis Investigative Site

Seoul, South Korea

Novartis Investigative Site

Seoul, South Korea

Novartis Investigative Site

Seoul, South Korea

Novartis Investigative Site

Seoul, South Korea

Novartis Investigative Site

Taegu, South Korea