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Completed
NCT05621733
A PMS of Jakavi® in Patients With Steroid-Refractory Graft-versus-Host Disease (SR-GvHD) in Korea
Conditions: Graft-versus-Host Disease
Sex: All
Ages: 12 Years – 100 Years
Healthy volunteers: No
Enrollment: 140
Sponsor: Novartis Pharmaceuticals
Location: Novartis Investigative Site Daegu Dalseo gu
Summary
This study is a prospective, open-label, multi-center, non-comparative, observational study to assess safety and effectiveness of Jakavi® (ruxolitinib) in the real-world clinical setting in Korean Graft-versus-Host disease (GvHD) patients
Eligibility Criteria
Inclusion Criteria:
1. Patients who diagnosed with GvHD and currently receiving or going to receive Jakavi® treatment according to locally approved label
2. Patients who are willing to provide written informed consent prior to study enrollment
Exclusion Criteria:
1. Patients under 12 years old
2. Patients with contraindication according to locally approved label of Jakavi®
3. Patients who receive or are going to receive any investigational medicine during the observation period.
Source: ClinicalTrials.gov (NCT05621733). StuddyBuddy aggregates publicly available trial information.