Abstract | OBJECTIVE: DESIGN: Multicenter, double-blind, randomized, placebo-controlled clinical trial. SETTING: Academic departments of dermatology in the United States. PARTICIPANTS: Forty-five individuals with chronic and severe AA affecting 50% to 95% of the scalp hair and resistant to previous therapies. Intervention Alefacept, a US Food and Drug Administration-approved T-cell biologic inhibitor for the treatment of moderate to severe plaque psoriasis. Main Outcome Measure Improved Severity of Alopecia Tool ( SALT) score over 24 weeks. RESULTS: Participants receiving alefacept for 12 consecutive weeks demonstrated no statistically significant improvement in AA when compared with a well-matched placebo-receiving group (P = .70). Conclusion Alefacept is ineffective for the treatment of severe AA.
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Authors | Bruce E Strober, Kavita Menon, Amy McMichael, Maria Hordinsky, Gerald Krueger, Jackie Panko, Kimberly Siu, Jonathan L Lustgarten, Elizabeth K Ross, Jerry Shapiro |
Journal | Archives of dermatology
(Arch Dermatol)
Vol. 145
Issue 11
Pg. 1262-6
(Nov 2009)
ISSN: 1538-3652 [Electronic] United States |
PMID | 19917955
(Publication Type: Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Dermatologic Agents
- Recombinant Fusion Proteins
- Alefacept
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Topics |
- Academic Medical Centers
- Adolescent
- Adult
- Aged
- Alefacept
- Alopecia Areata
(diagnosis, drug therapy)
- Dermatologic Agents
(administration & dosage)
- Dose-Response Relationship, Drug
- Double-Blind Method
- Drug Administration Schedule
- Female
- Follow-Up Studies
- Humans
- Injections, Intramuscular
- Male
- Middle Aged
- New York City
- Probability
- Recombinant Fusion Proteins
(administration & dosage)
- Risk Assessment
- Severity of Illness Index
- Statistics, Nonparametric
- Treatment Outcome
- Young Adult
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