Skip to content

A Study of Ruxolitinib in Patients With Graft-Versus Host Disease

Post-marketing Database Study in Patients With Graft-Versus Host Disease for JAKAVI Tablets

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07594587
Enrollment
395
Registered
2026-05-19
Start date
2026-05-11
Completion date
2030-05-15
Last updated
2026-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Graft-Versus-Host Disease

Keywords

Ruxolitinib, GVHD

Brief summary

This study aims to evaluate the safety and effectiveness of Jakavi® (ruxolitinib) in patients with acute graft-versus host disease (GVHD) and chronic GVHD in clinical practice.

Interventions

None listed

Sponsors

Novartis Pharmaceuticals
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with acute and chronic GVHD * Patients treated with ruxolitinib

Exclusion criteria

None Other protocol-defined inclusion/

Design outcomes

Primary

MeasureTime frameDescription
Number and Percentage of Patients With Common Terminology Criteria for Adverse Event (CTCAE) Grade ≥ 3 InfectionsUp to 1 yearGrade ≥ 3 infections according to the CTCAE v5.0.
Number and Percentage of Deaths Due to InfectionUp to 1 year
Time to First EventUp to 1 yearTime to first event is defined as the time from the start date of treatment with ruxolitinib to the first onset date of infection. Grade ≥ 4 infections according to the CTCAE v5.0.

Secondary

MeasureTime frameDescription
Number and Percentage of CTCAE Grade ≥ 3 InfectionsUp to 1 yearGrade ≥ 3 infections according to the CTCAE v5.0.
Odds Ratio of CTCAE Grade ≥ 3 InfectionsUp to 1 yearOdds ratios of infections and their 95% confidence intervals summarized by risk factors for infection.
Number and Percentage of Patients With Adverse Events Other Than InfectionsUp to 1 year
Number and Percentage of Patients who Died From Reasons Other Than InfectionUp to 1 year
Time to First Onset of Bone-related EventsUp to 1 yearThe time to the first onset is defined as the time from the start date of treatment with ruxolitinib to the first onset date of CTCAE Grade ≥ 4 fracture or bone-related events other than fracture.
Overall Response Rate (ORR) Among Patients With Acute GVHDDay 28ORR is defined as the proportion of patients with complete response (CR) or partial response (PR).
Number and Percentage of Stages of Disorder for Each Organ Among Patients With Acute GVHDBaseline, Day 28, up to 1 year
ORR Among Patients With Chronic GVHDMonth 6ORR is defined as the proportion of patients with CR or PR.
Number and Percentage of Chronic GVHD Patients by ResponseBaseline, Month 6, up to 1 yearResponse (CR, PR, mixed response, no change, progression) as entered into the database by the physician in accordance with the Japanese Society for Transplantation and Cellular Therapy guidelines for hematopoietic cell transplantation.
Best Overall Response (BOR)Baseline, up to 1 yearBOR is defined as the proportion of patients with CR or PR at any time point up to Month 12 of treatment.
Overall SurvivalUp to 1 yearOverall survival is defined as the time from the start date of treatment with ruxolitinib to the date of death due to any cause.
Duration of Response (DOR) Among Chronic GVHD PatientsUp to 1 yearDOR is defined for patients who achieved a response (CR or PR) by Month 12 of treatment as the time from the date of first documented response by Month 12 to the date of a DOR event (progression of chronic GVHD, death, or initiation of new systemic therapy for chronic GVHD, whichever occurs first).
Time to Response (TTR) Among Chronic GVHD PatientsUp to 1 yearTTR is defined as the time from the start date of treatment with ruxolitinib to the date of first confirmed response (CR or PR).

Countries

Japan

Contacts

CONTACTNovartis Pharmaceuticals
novartis.email@novartis.com+41613241111
STUDY_DIRECTORNovartis Pharmaceuticals

Novartis Pharmaceuticals

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 9, 2026