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. 1972 Dec;2(6):423-6.
doi: 10.1128/AAC.2.6.423.

Clotrimazole (Bay b 5097): in vitro and clinical pharmacological studies

Clotrimazole (Bay b 5097): in vitro and clinical pharmacological studies

M A Burgess et al. Antimicrob Agents Chemother. 1972 Dec.

Abstract

Clotrimazole (Bay b 5097) is a new synthetic antifungal drug with in vitro activity against Candida spp., Torulopsis glabrata, and Saccharomyces spp. Pharmacological studies in man after the oral administration of 1.5 and 3 g of clotrimazole produced mean peak concentrations in the serum of 1.16 and 1.29 mug/ml, respectively, 2 hr after administration. In six patients taking 1.5 g of clotrimazole every 6 hr, there was a progressive decline in the serum concentrations after administration of a dose on days 1, 4, and 8. Nine other patients begun on a similar schedule manifested gastrointestinal symptoms attributed to the clotrimazole and were unable to complete the study. Concentrations of active drug in the urine were less than 1% of the administered dose.

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