Assessment of the Safety, Tolerability and Efficacy of MEDI8968 in Subjects With Moderate to Severe Hidradenitis Suppurativa



Status:Completed
Conditions:Dermatology
Therapuetic Areas:Dermatology / Plastic Surgery
Healthy:No
Age Range:18 - 65
Updated:5/5/2014
Start Date:May 2013
End Date:September 2014
Contact:Kelly Webster, MS, MT(ASCP)
Email:ClinicalTrialTransparency@astrazeneca.com
Phone:+1 781 839 4324

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A Phase IIa Randomized, Double-Blind, Placebo-controlled, Multicenter Study to Assess the Safety, Tolerability and Preliminary Efficacy of MEDI8968 in Subjects With Moderate to Severe Hidradenitis Suppurativa

The purpose of this study is to gain initial evidence for the safety, tolerability and
efficacy of MEDI8968 for the treatment of subjects with moderate to severe hidradenitis
suppurativa


Inclusion Criteria:

- Hidradenitis suppurativa (HS) (moderate to severe)

- Diagnosis of HS for at least 1 year

- At least 5 active inflammatory lesions in at least 2 locations

- On a stable dose of antibiotics and/or analgesics for at least 4 weeks (if already
taking these medications)

- Average pain score of 3-9.

Exclusion Criteria:

- History of cyclic neutropenia

- Laboratory assessment abnormalities

- Underlying disorder considered unsuitable for inclusion

- Other skin diseases that may interfere with HS assessment

- Pregnancy or planning for pregnancy
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