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 |
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
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
We found this trial at
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