Immune Thrombocytopenia Clinical Trial
Official title:
A Prospective, Multicenter Study on the Alteration of Different Immune Parameters in ITP Patients Receiving Eltrombopag Treatment.
This project was undertaken by Qilu Hospital of Shandong University and other well-known hospitals in China. In order to report the alteration of Different Immune Parameters in ITP Patients Receiving Eltrombopag Treatment.
The primary objective of this study is to determine the efficacy of oral eltrombopag as a
thrombopoietic agent treating previously treated chronic Chinese ITP patients and
investigate the alteration of Different Immune Parameters after eltrombopag therapy.
Approximately 30 eligible subjects with primary ITP who have not responded to or have
relapsed after previous treatment for ITP will be selected. The initial dose of eltrombopag
administration is 25 mg orally once daily. During the 6 weeks follow-up, dose of
investigational product will be adjusted according to the weekly subject platelet count, and
a battery of immune parameters will be monitored at the end of each week. Additionally, the
efficacy of oral eltrombopag for ITP will be assessed after 6 weeks administration.
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Observational Model: Cohort, Time Perspective: Prospective
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