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The Clinical Trials Supporting Benzyl Alcohol Lotion 5% (Ulesfia TM ): A Safe and Effective Topical Treatment for Head Lice (Pediculosis Humanus Capitis)
Author(s) -
Meinking Terri L.,
Villar Maria E.,
Vicaria Maureen,
Eyerdam Debbie H.,
Paquet Diane,
MertzRivera Kamara,
Rivera Hector F.,
Hiriart Javier,
Reyna Susan
Publication year - 2010
Publication title -
pediatric dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.542
H-Index - 73
eISSN - 1525-1470
pISSN - 0736-8046
DOI - 10.1111/j.1525-1470.2009.01059.x
Subject(s) - lotion , medicine , clinical trial , placebo , dermatology , surgery , pharmacology , pathology , alternative medicine
Benzyl alcohol lotion 5% (BAL 5%) is a non‐neurotoxic topical head lice treatment that is safe and effective in children as young as 6 months of age. The safety and efficacy of this pediculicide has been studied in 695 (confirm number) subjects in all phases of clinical development. Scanning electron micrographs (SEM) demonstrated that the active agent appears to stun the breathing spiracles open, enabling the vehicle to penetrate the respiratory mechanism (spiracles), therefore asphyxiating the lice. Initial phase II trials compared this novel product to RID ® using identical volumes of treatment (4 oz/application) and yielding, almost, identical efficacy. This outcome pointed to the significant importance of completely saturating the hair with the product in order to achieve maximum treatment success. A second phase II trial, which allowed the use of sufficient product to saturate the hair, resulted in 100% efficacy after both 10 and 30 minute treatments. A third phase II trial verified an effective dose. Phase III trials compared BAL 5% to vehicle placebo for two 10‐minute applications. It proved to be safe and effective (p < 0.001) for treatment of head lice and is the first FDA‐approved non‐neurotoxic lice treatment, now available in the United States as Ulesfia TM lotion.