Published in Clinical Trials Week, November 9th, 2009
"We sought to determine the safety, including the dose-limiting toxicities with adverse events, and efficacy, ie, response rate, of bexarotene in alopecia areata. We conducted a phase I/II randomized, half-head trial of 1% bexarotene gel applied twice daily for 6 months. In all, 42 patients (11 male and 31 female) with alopecia totalis (n = 3), alopecia universalis (n = 5), or alopecia areata (n = 34) applied 1% bexarotene gel for 24 weeks. Five of...
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Source: Clinical Trials Week (2009-11-09)
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