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Clinical trialNCT01317875CompletedPhase 1Interventional

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)

SponsorIncyte CorporationEnrollment69Myelofibrosis
View the registry record on ClinicalTrials.gov

Summary

The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

18 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Austria
  • Facility name not stated

    Vienna, Austria

China
  • Facility name not stated

    Nanjing, Jiangsu, China

  • Facility name not stated

    Chengdu, Sichuan, China

  • Facility name not stated

    Hangzhou, Zhejiang, China

  • Facility name not stated

    Beijing, China

France
  • Facility name not stated

    Angers, France

  • Facility name not stated

    Paris, France

  • Facility name not stated

    Pierre-Bénite, France

Germany
  • Facility name not stated

    Leipzig, Germany

Italy
  • Facility name not stated

    Florence, Italy

  • Facility name not stated

    Milan, Italy

  • Facility name not stated

    Terni, Italy

Netherlands
  • Facility name not stated

    Rotterdam, Netherlands

United Kingdom
  • Facility name not stated

    Belfast, United Kingdom

  • Facility name not stated

    London, United Kingdom

United States
  • Facility name not stated

    Winter Park, Florida, United States

  • Facility name not stated

    Baltimore, Maryland, United States

  • Facility name not stated

    Houston, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Mar 2011
Primary completion
31 Dec 2019
Completion
31 Dec 2019
Last update posted
22 Aug 2025
Registered enrollment
69
Registry id
NCT01317875

Cross-registrations

EU-CTR / CTIS (EudraCT)2010-023055-29

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.