drugset / Trial / NCT07051915

Summary

This study is a phase 3 study where eligible patients will be randomized 1:1 to one of two treatment strategies: receiving a thrombopoietin receptor agonist (Avatrombopag), or anti-CD20 (Rituximab).

Timeline

Start
2025-09-15
Primary completion
2028-01-31
Completion
2029-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Avatrombopag Small molecule 20 mg Oral
Subject Rituximab Monoclonal antibody 1000 mg Intravenous