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Study identifier: NCT06462469 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of Efficacy and Safety of Ruxolitinib in Patients With Grade II to IV Steroid-refractory Acute Graft vs. Host Disease

Condition: Steroid-refractory Acute Graft Versus Host Disease  ·  Sponsor: Novartis Pharmaceuticals

PhasePhase 4
Planned participants36
Who can joinAll sexes, 12 Years to 100 Years
Healthy volunteersNo

About this study

The purpose of this study is to assess the efficacy and safety of ruxolitinib therapy in Chinese adults and adolescents (≥ 12 years old) with Grade II-IV steroid-refractory acute graft versus host disease (SR-aGvHD).

This description comes directly from the study's public registry record.

Talk to the study team

Novartis Pharmaceuticals  ·  +41613241111  ·  novartis.email@novartis.com

Novartis Pharmaceuticals

Always discuss trial participation with your own doctor first.

Locations (17)

Novartis Investigative SiteGuangzhou, Guangdong, ChinaRecruiting
Novartis Investigative SiteGuangzhou, Guangdong, ChinaRecruiting
Novartis Investigative SiteZhengzhou, Henan, ChinaRecruiting
Novartis Investigative SiteWuhan, Hubei, ChinaRecruiting
Novartis Investigative SiteChangchun, Jilin, ChinaRecruiting
Novartis Investigative SiteXian, Shanxi, ChinaRecruiting
Novartis Investigative SiteChengdu, Sichuan, ChinaRecruiting
Novartis Investigative SiteHangzhou, Zhejiang, ChinaRecruiting
Novartis Investigative SiteBeijing, ChinaRecruiting
Novartis Investigative SiteBeijing, ChinaRecruiting
Novartis Investigative SiteBeijing, ChinaRecruiting
Novartis Investigative SiteBeijing, ChinaRecruiting

+ 5 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06462469