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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.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05621733). StuddyBuddy aggregates publicly available trial information.