drugset / Trial / NCT01516749

Anakinra as a Treatment for Hydradenitis Suppurativa

NCT01516749 ↗

Phase 2 Completed 6 enrolled University of California, San Francisco
NaSingle-groupOpen-labelTreatment

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.

Timeline

Start
2012-10
Primary completion
2013-05
Completion
2013-07

Outcome

Met primary endpoint

registry MEAN Anakinra: -34.8 (-62.05 to -7.56) units on a scale NCT01516749 ↗

registry analysis (superiority or other test); Anakinra; p = 0.024; t-test, 2 sided; note: significance was accepted at p\<0.05 NCT01516749 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Anakinra Protein / enzyme biologic 100 mg Subcutaneous