drugset / Trial / NCT06281327

Summary

To evaluate the safety and efficacy of avatrombopag in the treatment of pediatric primary immune thrombocytopenia in patients who have been treated with eltrombopag before and switched to avatrobopag because of poor efficacy, excessive platelet fluctuation or intolerance, or patient preference, economic reasons, and other reasons.

Timeline

Start
2024-03-01
Primary completion
2025-12
Completion
2025-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Avatrombopag Small molecule 10 mg Oral
Subject Avatrombopag Small molecule 20 mg Oral
Subject Avatrombopag Small molecule 40 mg Oral