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

PHASE2CompletedINTERVENTIONAL
Enrollment

115

Participants

Timeline

Start Date

January 15, 2023

Primary Completion Date

October 10, 2024

Study Completion Date

December 1, 2024

Conditions
Transplant-Related Disorder
Interventions
DRUG

Ruxolitinib

"Model-predicted high-risk patients: ruxolitinib 5mg bid po until at least day 60 post-transplant and terminated after day 100. If severe hematological signs occur such as when there is severe neutropenia (\<0.1×10\^9/L), ruxolitinib can be used at half dose or discontinued as appropriate, and can continue to be used after hematology recovery.~Model-predicted moderate-risk patients: ruxolitinib 2.5mg bid p po until at least day 60 post-transplant and terminated after day 100. If severe hematological signs occur such as when there is severe neutropenia (\<0.1×10\^9/L), ruxolitinib can be used at half dose or discontinued as appropriate, and can continue to be used after hematology recovery.~Model-predicted low risk: regular aGVHD prophylactic regimens."

Trial Locations (1)

300020

Institute of Hematology & Blood Diseases Hospital, Tianjin

All Listed Sponsors
lead

Institute of Hematology & Blood Diseases Hospital, China

OTHER