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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
70
from 0.5mg twice a day to maximally increase total10mg in 8 weeks and maintain maximal tolerable dose to 104 weeks
National Health Insurance Service Ilsan Hospital
Goyang-si, Gyeonggi-do, South Korea
The Catholic University of Korea. ST. Vincents Hospital
response rate for less than 60 X 10^4/ul in platelet count
Time frame: at week 8
response rate for less than 60 X 10^4/ul in platelet count
Time frame: at week 52
changes from baseline in 50% reduction rate in platelet count
Time frame: up to 52 weeks
response rate for less than 40 X 10^4/ul in platelet count
Time frame: up to 52 weeks
cumulative incidence of essential thrombocythemia related events (e.g thromboembolic or hemorrhagic events)
Time frame: at 52 week
incidence of adverse events
Time frame: up to 52 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Suwon, Gyeonggi-do, South Korea
Hallym UNIV. Medical Center
Anyang, South Korea
Daegu Catholic University Medical Center
Daegu, South Korea
Keimyung University Dongsan Medical Center
Daegu, South Korea
Kyungpook national university hospital
Daegu, South Korea
Dongguk University Medical Center
Goyang, South Korea
Cheonnam National University Hwasun Hospital
Hwasun, South Korea
Gachon University Gil Medical Center
Incheon, South Korea
Inha University Hospital
Incheon, South Korea
...and 11 more locations