Exploratory Multi-centre Trial In Patients With ET Treated With XAGRID®

NCT01352585 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 47

Last updated 2021-07-30

Study results available
· View outcomes & findings →

Summary

This study is hypothesis-generating to explore the impact of JAK2 (V617F) mutation status on the treatment response to anagrelide hydrochloride

Conditions

  • Essential Thrombocythemia (ET)

Interventions

DRUG

Anagrelide hydrochloride

0.5 mg hard capsules, dosing decisions will be made by the treating physician

Sponsors & Collaborators

  • Shire

    lead INDUSTRY

Principal Investigators

  • Study Director · Takeda

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-07-19
Primary Completion
2013-09-19
Completion
2013-09-19

Countries

  • Italy

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01352585 on ClinicalTrials.gov