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Not Yet RecruitingNCT07067099

Neutralizing Interferon Type 1 in Hidradenitis Suppurativa

Use of Plasma With Neutralizing Autoantibodies to Type I Interferons in Patients With Severe Refractory Flare-up of Hidradenitis Suppurativa

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
6 (estimated)
Sponsor
Centre Hospitalier Universitaire de Besancon · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to evaluate the safety and type 1 Interferon (IFN) neutralization in patients with refractory severe Hidradenitis Suppurativa (Hurley stage III) after transfusion of plasma containing high titer anti-IFN-1 autoantibodies.

Conditions

Interventions

TypeNameDescription
BIOLOGICALPlasma with neutralizing autoantibodies to Type I InterferonsTransfusion of one unit of plasma containing high titre anti-IFN-1 autoantibodies

Timeline

Start date
2025-09-01
Primary completion
2026-06-01
Completion
2026-09-01
First posted
2025-07-16
Last updated
2025-07-16

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT07067099. Inclusion in this directory is not an endorsement.

Neutralizing Interferon Type 1 in Hidradenitis Suppurativa (NCT07067099) · Clinical Trials Directory