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NCT06660329

Efficacy and Safety of Tofacitinib in Refractory Blau Syndrome

ENROLLING BY INVITATION Phase 4 Last updated 28 October 2024
What this trial tests

Phase 4 trial testing Janus Kinase Inhibitor in Blau Syndrome in 30 participants. Enrolling by invitation.

Timeline
1 October 2024
Primary endpoint
1 October 2027
1 October 2028

Quick facts

Lead sponsorPeking Union Medical College Hospital
PhasePhase 4
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment30
Start date1 October 2024
Primary completion1 October 2027
Estimated completion1 October 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking Union Medical College Hospital

Who can join

Adults 0 to 18, any sex, with Blau Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a prospective cohort study to observe the efficacy and safety of Tofacitinib in children with Blau syndrome (BS). The investigators would analyze the rate of remission or low disease activity after treatment as well as changes in inflammatory markers, patients' and physician's global assessment of disease activity to determine the efficacy and safety of Tofacitinib.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Janus Kinase Inhibitor

Trials testing the same drug.

Other recruiting trials for Blau Syndrome

Currently open trials in the same condition.

Other Peking Union Medical College Hospital 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/NCT06660329.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing