RecruitingNCT06665412
Efficacy and Safety of Dose Redution of Radotinib as a First Line Treament in Ph+ CML
Studying Chronic myeloid leukemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Il-Yang Pharm. Co., Ltd.
- Principal Investigator
- Na Yun KimIl-Yang Pharm. Co., Ltd.
- Intervention
- Radotinib Hydrochloride(drug)
- Enrollment
- 168 enrolled
- Eligibility
- 19 years · All sexes
- Timeline
- 2024 – 2026
Study locations (2)
- Hallym University Sacred Heart Hosptial, Anyang-si, Gyeonnggi-do, South Korea
- Keimyung University Daegu Dongsan Hospital, Daegu, South Korea
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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