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NCT07588945
daGOAT-Guided Prevention of Severe aGVHD After Allo-HSCT
Conditions: Transplant-Related Disorder
Sex: All
Ages: 16 Years – N/A
Healthy volunteers: No
Phase: PHASE3
Enrollment: 438
Sponsor: Institute of Hematology & Blood Diseases Hospital, China
Summary
This study aims to evaluate the efficacy of prophylactic ruxolitinib in adult patients at intermediate-to-high risk of severe acute GvHD, as predicted by the daGOAT model.
Eligibility Criteria
Inclusion Criteria:
1. Age \> 16 years old.
2. HLA-haploidentical transplant.
3. Able to take oral medications.
4. Patients must provide written informed consent before the start of the study procedures.
Exclusion Criteria:
1. Patients who have undergone tandem transplantation or multiple transplantations.
2. Patients who are allergic to or cannot tolerate ruxolitinib.
3. Patients with mental or other medical conditions that make them unable to comply with the study treatment and monitoring requirements.
4. Patients who are ineligible for the study due to other factors, or who will bear great risk if they participate in the study.
Source: ClinicalTrials.gov (NCT07588945). StuddyBuddy aggregates publicly available trial information.
