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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Key facts

Sponsor
Il-Yang Pharm. Co., Ltd.
Principal Investigator
Na Yun Kim
Il-Yang Pharm. Co., Ltd.
Intervention
Radotinib Hydrochloride(drug)
Enrollment
168 enrolled
Eligibility
19 years · All sexes
Timeline
20242026

Study locations (2)

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.

Open NCT06665412 on ClinicalTrials.gov

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