Active, not recruitingPHASE1, PHASE2NCT04446650
A Study of Fedratinib in Japanese Subjects With DIPSS (Dynamic International Prognostic Scoring System)- Intermediate or High-risk Primary Myelofibrosis (PMF), Post-polycythemia Vera Myelofibrosis (Post-PV MF), or Post-essential Thrombocythemia Myelofibrosis (Post-ET MF)
Studying Essential thrombocythemia
Last synced from ClinicalTrials.gov
ℹ
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
- 31 enrolled
- Eligibility
- 20 years · All sexes
- Timeline
- 2020 – 2026
Study locations (21)
- Local Institution - 021, Suwa, Nagano, Japan
- Local Institution - 001, Bunkyo-ku, Tokyo, Japan
- Local Institution - 006, Chūō, Yamanashi, Japan
- Local Institution - 002, Aomori, Japan
- Local Institution - 004, Bunkyō City, Japan
- Local Institution - 015, Fukuoka, Japan
- Local Institution - 018, Hitachi, Ibaraki, Japan
- Local Institution - 005, Isehara City, Kanagawa, Japan
- Local Institution - 010, Kamogawa, Japan
- Local Institution - 017, Kitakyushu, Japan
- Local Institution - 020, Kumamoto, Japan
- Local Institution - 013, Maebashi, Japan
- Local Institution - 012, Miyazaki, Japan
- Local Institution - 009, Nagasaki, Japan
- Local Institution - 016, Osaka, Japan
- +6 more locations on ClinicalTrials.gov
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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