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NOT YET RECRUITING
NCT07067099
PHASE1

Neutralizing Interferon Type 1 in Hidradenitis Suppurativa

Sponsor: Centre Hospitalier Universitaire de Besancon

View on ClinicalTrials.gov

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.

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

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

6

Start Date

2025-09

Completion Date

2026-09

Last Updated

2025-07-16

Healthy Volunteers

No

Interventions

BIOLOGICAL

Plasma with neutralizing autoantibodies to Type I Interferons

Transfusion of one unit of plasma containing high titre anti-IFN-1 autoantibodies

Locations (1)

CHU Besançon

Besançon, France