RecruitingNCT06073847
A Post-Marketing Surveillance Study to Assess the Safety of Fedratinib in Korean Patients With Myelofibrosis
Studying Essential thrombocythemia
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
- Bristol-Myers Squibb
- Principal Investigator
- Bristol-Myers SquibbBristol-Myers Squibb
- Intervention
- Fedratinib(drug)
- Enrollment
- 137 enrolled
- Eligibility
- 19 years · All sexes
- Timeline
- 2023 – 2027
Study locations (3)
- Bristol-Myers Squibb YH, Seoul, South Korea
- Local Institution - 0001, Seoul, South Korea
- Novotech Laboratory Korea Co., Ltd., Seoul, 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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