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)

PHASE1CompletedINTERVENTIONAL
Enrollment

69

Participants

Timeline

Start Date

March 31, 2011

Primary Completion Date

December 31, 2019

Study Completion Date

December 31, 2019

Conditions
Myelofibrosis
Interventions
DRUG

Ruxolitinib

"Starting dose of ruxolitinib for cohort 1 in dose escalation phase - 5mg twice a day (BID)~Doses will be increased a total of approximately 5mg for successive dosing cohorts based on baseline platelet count"

Trial Locations (18)

21229

Baltimore

32789

Winter Park

77030

Houston

Unknown

Vienna

Nanjing

Chengdu

Hangzhou

Beijing

Angers

Paris

Pierre-Bénite

Leipzig

Florence

Milan

Terni

Rotterdam

Belfast

London

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Novartis

INDUSTRY

lead

Incyte Corporation

INDUSTRY

NCT01317875 - 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) | Biotech Hunter | Biotech Hunter