drugset / Trial / NCT03538041

A Study of INCB050465 in Participants With Autoimmune Hemolytic Anemia

NCT03538041 ↗

Phase 2 Completed 25 enrolled Incyte Corporation
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and efficacy of parsaclisib administered orally to participants with autoimmune hemolytic anemia (AIHA) who have decreased hemoglobin and evidence of ongoing hemolysis that requires treatment intervention.

Timeline

Start
2018-11-21
Primary completion
2021-08-05
Completion
2024-04-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Parsaclisib Unknown 1 mg Oral
Subject Parsaclisib Unknown 2.5 mg Oral