Anakinra as a Treatment for Hydradenitis Suppurativa

Status Completed

Clinical Trial Summary

This is an open-label, proof-of-concept research study to assess the effectiveness of anakinra in the treatment of patients with hidradenitis suppurativa (HS). The planned intervention is to provide about 6 HS patients with anakinra 100mg daily injections to administer subcutaneously for 8 weeks. Then, the study subjects will be followed for a further 8 weeks to monitor for relapse of HS.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01516749
Study type	Interventional
Source	University of California, San Francisco
Contact
Status	Completed
Phase	Phase 2
Start date	October 2012
Completion date	July 2013

View Details

See also
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