1. Academic Validation
  2. In vivo efficacy of SM-8668 (Sch 39304), a new oral triazole antifungal agent

In vivo efficacy of SM-8668 (Sch 39304), a new oral triazole antifungal agent

  • Antimicrob Agents Chemother. 1990 Jun;34(6):980-4. doi: 10.1128/AAC.34.6.980.
T Tanio 1 K Ichise T Nakajima T Okuda
Affiliations

Affiliation

  • 1 Research Laboratories, Sumitomo Pharmaceuticals Co., Ltd., Osaka, Japan.
Abstract

SM-8668 (Sch 39304) is a new oral Antifungal agent which we evaluated in comparison with fluconazole in various fungal Infection models. The prophylactic effect of SM-8668 was excellent against systemic candidiasis, aspergillosis, and cryptococcosis in mice. The 50% effective dose for SM-8668 was assessed at 10 days after Infection and was 0.18, 3.7, and 5.9 mg/kg (body weight), respectively, for the above-mentioned Fungal diseases. Fluconazole was about four times less effective than SM-8668 against systemic candidiasis and was only slightly effective at doses of 80 and 25 mg/kg against systemic aspergilosis and cryptococcosis, respectively. SM-8668 was also about four to eight times more active than fluconazole against vaginal candidiasis in rats and against dermatophytic Infection in guinea pigs. In addition, topical SM-8668 was as effective as topical miconazole or tioconazole against skin mycosis in guinea pigs. After oral administration, SM-8668 showed a maximum concentration in serum similar to that of fluconazole in both mice and rats, but the elimination half-life and area under the serum concentration-time curve for SM-8668 were twice those for fluconazole.

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