| Literature DB >> 6285709 |
R E Keeney, L E Kirk, D Bridgen.
Abstract
Acyclovir tolerance has been explored in a broad range of human populations and dosage regimens with intravenous, topical, and oral formulations. Phase I pharmacokinetic/tolerance studies assured safety in special populations at unique risk of complicated herpes infections who were simultaneously at increased risk of toxicity to anti-DNA chemotherapeutic agents. Further safety evaluations accompanied placebo-controlled Phase II studies in infected patients who represent future users of acyclovir. These studies confirm acyclovir as the safest antiherpes agent to be explored in clinical studies to date.Entities:
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Year: 1982 PMID: 6285709 DOI: 10.1016/0002-9343(82)90086-9
Source DB: PubMed Journal: Am J Med ISSN: 0002-9343 Impact factor: 4.965