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Antimicrobial Agents and Chemotherapy, Sep 1997, 1961-1964, Vol 41, No. 9
DI Bernstein, CJ Schleupner, TG Evans, DA Blumberg, Y Bryson, K Grafford, P Broberg, S Martin-Munley and SL Spruance
A topical 3% foscarnet cream formulation was evaluated for its ability to
treat experimental UV radiation (UVR)-induced herpes labialis in a
double-blind study. Healthy adult volunteers with a history of sunlight-
induced herpes labialis were randomly assigned at four centers to receive
either foscarnet cream (n = 152) or a vehicle control (n = 150). Following
measurement of the minimal erythematous dose (MED), the subjects' lips were
exposed to 4 MEDs of UV light. Subjects applied the cream on the
UVR-exposed area approximately eight times daily beginning immediately
after UVR exposure and continuing for 7 days, or until all lesions had a
minimum of 4 days of treatment. There were no significant differences
between groups in the percentages of subjects that developed any lesion,
aborted lesions (did not progress beyond a papule), immediate lesions
(developed within 48 h of UVR), or delayed classic lesions (developed 48 h
to 7 days after UVR). Treatment with foscarnet significantly reduced the
mean lesion area (49 versus 81 mm2; P = 0.01), the maximum lesion area (80
versus 141 mm2; P = 0.01), and the time to healing (P = 0.03) of the
delayed classic lesions (n = 78). There was also a trend for a decrease in
the mean duration of these lesions (156 versus 191 h; P = 0.08) and the
duration of pain (3.9 versus 4.3 days; P = 0.06) in foscarnet-treated
subjects. There were no clinically significant adverse reactions. These
data suggest that topical foscarnet can be efficacious and deserves further
evaluation for the treatment of herpes labialis.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Effect of foscarnet cream on experimental UV radiation-induced herpes labialis
Division of Infectious Diseases, Children's Hospital Medical Center, Cincinnati, Ohio 45229-3039, USA. dib@chmcc.org
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