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Asciminib RMP Study
Asciminib RMP Study

NCT05943522

RecruitingN/A

Sponsor: Novartis Pharmaceuticals

Conditions: Chronic Myeloid Leukemia

Interventions: Asciminib

Countries: South Korea

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 overview

Sex: ALL

Age: 18 Years to 100 Years

Healthy volunteers: No

Study type: OBSERVATIONAL

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
Locations (17)
  • Wŏnju, Gangwon-do, South Korea
  • Anyang-si, Gyeonggi-do, South Korea
  • Bucheon-si, Gyeonggi-do, South Korea
  • Uijeongbu-si, Gyeonggi-do, South Korea
  • Gyeonggi-do, Korea, South Korea
  • Incheon, Korea, South Korea
  • Seoul, Korea, South Korea
  • Seoul, Seoul, South Korea
  • Seoul, Seoul, South Korea
  • Seoul, Yangcheon gu, South Korea
  • Suwon, Yeongtong Gu, South Korea
  • Jeollanam, South Korea
  • Pusan, South Korea
  • Seoul, South Korea
  • Seoul, South Korea
  • Seoul, South Korea
  • Taegu, South Korea