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NCT03701698

Ruxolitinib and Steroid As First Line Therapy for Acute GVHD

Terminated Phase 2 Last updated 1 October 2024
What this trial tests

Phase 2 trial testing Ruxolitinib Oral Tablet in Acute GVHD in 1 participant. Terminated before completion.

Timeline
1 November 2018
Primary endpoint
20 September 2024
20 September 2024

Quick facts

Lead sponsorShanghai General Hospital, Shanghai Jiao Tong University School of Medicine
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeprevention
Enrollment1
Start date1 November 2018
Primary completion20 September 2024
Estimated completion20 September 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

Who can join

Adults 18 to 70, any sex, with Acute GVHD. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the efficacy of ruxolitinib in combination with methylprednisolone as first line therapy in patients with Grades II to IV acute graft-versus-host disease (GVHD).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Challenges and opportunities targeting mechanisms of epithelial injury and recovery in acute intestinal graft-versus-host disease.
    Jansen SA, Nieuwenhuis EES, Hanash AM, Lindemans CA. · · 2022 · cited 24× · PMID 35654837 · DOI 10.1038/s41385-022-00527-6

Verify or expand the search:

Other trials of Ruxolitinib Oral Tablet

Trials testing the same drug.

Other recruiting trials for Acute GVHD

Currently open trials in the same condition.

Other Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03701698.

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