Graft Versus Host Disease (GvHD) Clinical Trials

Find Graft Versus Host Disease (GvHD) Clinical Trials Near You

A Nation-wide, Multi-center, Prospective, Randomized, Parallel-group, Open-label, Investigator Initiated Pilot Study to Evaluate Efficacy and Safety of Systemic Corticosteroid Plus Ruxolitinib as First-line Therapy in Patients With New-onset Moderate to Severe Chronic Graft-versus-host Disease

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Chronic graft-versus-host disease (cGVHD) is a complication that occurs in 30-40% of recipients of allogeneic hematopoietic stem cell transplantation (allo-HSCT) and is a major cause of late non-relapse mortality. In cases where the initial treatment response is inadequate, irreversible tissue damage often persists, making it a fatal complication that significantly reduces quality of life even for long-term survivors. Therefore, the success of first-line treatment is crucial, but to date, there are no approved drugs specifically for the first-line treatment of chronic graft-versus-host disease. Besides corticosteroids, which have been used palliatively for over 50 years, there are no proven effective treatments available. Against this background, this study was designed to explore the potential of new treatments as first-line therapy for chronic graft-versus-host disease, where effective treatment options are currently lacking. Initially, the objective response rate will be analyzed at the 48-week mark based on the NIH Consensus Criteria (Lee 2015). Additionally, the study will evaluate the proportion of patients with steroid-resistant or steroid-dependent conditions, the objective response rate(ORR), failure-free survival(FFS), duration of response(DOR), and the proportion of patients who have reduced corticosteroids. Furthermore, the differences in treatment effects between the two groups of patients will be analyzed based on safety endpoints, including adverse events, laboratory tests, physical examinations, and vital signs.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Healthy Volunteers: f
View:

• Adult men and women aged 19 or older based on the date of signing on the informed consent form

• On the screening visit, those who are diagnosed of a moderate to severe chronic graft-versus-host disease according to 2014 NIH consensus criteria

⁃ Moderate: At least one of the following conditions: \>1 point for at least three organs \>2 points for at least one organ except the lungs \>1 point for the lungs

⁃ Severe: At least one of the following conditions: \>3 points for at least one organ

⁃ At least 2 points for the lungs

• Those who have no history of systemic treatment for chronic graft-versus-host disease and now need systemic corticosteroid treatment

• Those whose ECOG (Eastern Cooperative Oncology Group) performance status is 0 to 2.

• Regardless of the donor (matched sibling-family donor, matched unrelated donor, or partially matched family donor), those who have successfully taken same-type stem cell transplantation (alloSCT) from the marrow, peripheral blood stem cell, or cord blood

• Those who voluntarily agree on participation in this clinical trial

Locations
Other Locations
Republic of Korea
The Catholic University of Korea, Seoul St. Mary's Hospital
RECRUITING
Seoul
Contact Information
Primary
ByungSik Cho, M.D. & Ph.D.
cbscho@catholic.ac.kr
+82-2-2258-6072
Time Frame
Start Date: 2025-01-15
Estimated Completion Date: 2029-08-31
Participants
Target number of participants: 88
Treatments
Experimental: Prednisone + Jakavi(ruxolitinib)
The experimental group will receive ruxolitinib 10 mg orally twice daily (BID) and prednisone (or equivalent) at a dosage of 1 mg/kg/day.~Subjects are orally administered with an investigational medicinal product (IMP) according to their designated treatment group for 48 weeks, and the investigator may adjust the dosage of IMPs based on symptoms of the target disease. (However, after the 48-week mark, participants in the ruxolitinib treatment group may continue to receive ruxolitinib for an additional maximum of 2 years, based on the investigator's judgment regarding the need for ongoing treatment. The total duration of ruxolitinib administration will not exceed 3 years.)
Active_comparator: Prednisone
The control group will receive prednisone (or equivalent) at a dosage of 1 mg/kg/day.~Subjects are orally administered with an investigational medicinal product (IMP) according to their designated treatment group for 48 weeks, and the investigator may adjust the dosage of IMPs based on symptoms of the target disease.
Related Therapeutic Areas
Sponsors
Leads: Byung-Sik Cho
Collaborators: Novartis

This content was sourced from clinicaltrials.gov