This study takes place within the Institute of Hematology & Blood Diseases Hospital and is a prospective, open-label, nonrandomized, multi-center trial designed to compare the efficacy and safety of using eltrombopag with low-dose rituximab vs the best available therapy (therapy not consisting of eltrombopag coupled with rituximab) for adults between 18-65 years of age who have autoantibody failure due to intolerance or resistance to first-line therapy options. Participants with secondary ITP will be included. Participants will be excluded from participating if they have active secondary thyroid disease or have a psychiatric disorder clinically diagnosed. Participants who have had rituximab in the last six months, or who have had any thromboses (clots) or are at a higher risk for thrombosis will also be excluded from participation.
China
Recruiting
