drugset / Trial / NCT03232177

Anagre Cap. in Patients With High-Risk Essential Thrombocythemia

NCT03232177

Phase 4 Completed 70 enrolled Yuhan Corporation
NaSingle-groupOpen-labelTreatment

Summary

This study is to evaluate the efficacy and safety according to incremental dosing for 8 weeks and duration of administration for 1 year in patients with high-risk essential thrombocythemia.

Timeline

Start
2017-06-05
Primary completion
2020-12-05
Completion
2020-12-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Anagrelide Small molecule 10 mg