| Literature DB >> 2111252 |
R J Ancill1, Y Takahashi, Y Kibune, R Campbell, J R Smith.
Abstract
In a randomized, double-blind, parallel group trial conducted in eight European centres, the 5-lipoxygenase inhibitor AA-861 was administered orally, starting 2 weeks before the pollen season and continuing for 8 weeks; after the start of the season escape medication was permitted if necessary. Patients were enrolled who had a previous history of pollen allergy, confirmed by skin prick tests and/or relevant allergen-specific immunoglobulin E to pollen. Daily symptoms scores were recorded on diary cards and assessments were made by the investigator during the study period. Better global improvement ratings were achieved using AA-861, as assessed both by the investigators and the patients. The total nasal symptoms scores and activities of daily living were also improved compared to placebo. No significant adverse reactions were encountered.Entities:
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Year: 1990 PMID: 2111252 DOI: 10.1177/030006059001800202
Source DB: PubMed Journal: J Int Med Res ISSN: 0300-0605 Impact factor: 1.671