drugset / Trial / NCT05600855

Prevention of Severe Acute Graft-versus-host Disease in Adult Patients Using a daGOAT Model

NCT05600855 ↗

NaSingle-groupOpen-labelPrevention

Summary

To evaluate the efficacy and safety of ruxolitinib for prophylactic therapy of adult patients who are predicted to have a high risk for developing severe acute graftversus-host disease (aGVHD) by the dynamic aGVHD Onset Anticipation Tianjin (daGOAT) model.

Timeline

Start
2023-01-15
Primary completion
2024-10-10
Completion
2024-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruxolitinib Small molecule 2.5 mg Oral
Subject Ruxolitinib Small molecule 5 mg Oral