CompletedPhase 1NCT01317875
Study of the JAK Inhibitor Ruxolitinib Administered Orally to Patients With Primary Myelofibrosis (PMF), Post-Polycythemia Vera-Myelofibrosis (PPV-MF) or Post-Essential Thrombocythemia-Myelofibrosis (PET-MF)
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
- Incyte Corporation
- Principal Investigator
- Mark Jones, MDIncyte Corporation
- Intervention
- Ruxolitinib(drug)
- Enrollment
- 69 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2011 – 2019
Study locations (18)
- Winter Park, Florida, United States
- Baltimore, Maryland, United States
- Houston, Texas, United States
- Vienna, Austria
- Nanjing, Jiangsu, China
- Chengdu, Sichuan, China
- Hangzhou, Zhejiang, China
- Beijing, China
- Angers, France
- Paris, France
- Pierre-Bénite, France
- Leipzig, Germany
- Florence, Italy
- Milan, Italy
- Terni, Italy
- +3 more locations on ClinicalTrials.gov
Collaborators
Novartis
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 NCT01317875 on ClinicalTrials.govOther trials for Essential thrombocythemia
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