The purpose of this study is to obtain information on efficacy, safety and Pharmacokinetics (PK)/Pharmacodynamics (PD) of Hetrombopag over 14 days in Chinese patients with chronic ITP.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
24
Hetrombopag Olamine 2.5mg, 5mg and 7.5mg
West Hospital, Sichuan University
Chengdu, China
RECRUITINGThe number of volunteers with adverse events as a measure of safety and tolerability
Time frame: up to Day 28
Plasma pharmacokinetic (PK) parameters of Hetrombopag after multiple dose from day 1 to day 14, composite including AUC, Cmax, Tmax, and t1/2
Time frame: day 1 and day 14
The proportion of patients with platelet counts ≥50,000/µL after treatment
Time frame: up to Day 28
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