Bax R, Douville K, McCormick D, Rosenberg M, Higgins J, Bowden M
Biosyn, Inc, 1800 Byberry Road, Building 13, Huntingdon Valley, PA 19006, USA.
Contraception. 2002 Nov;66(5):365-8. doi: 10.1016/s0010-7824(02)00389-x.
Despite a significant worldwide need for effective microbicides to reduce sexually transmitted diseases (STD) and HIV transmission, none is currently available. C31G, a surface active anti-infective agent that is active in vitro against bacterial and viral STD pathogens, was evaluated in a 3-day, once-daily dosing clinical trial designed to assess multiple formulations for safety and acceptance. The trial used a scoring algorithm that was based on relevant subject reported symptoms and signs observed at follow-up. Differences in tolerance and acceptability between the formulations were demonstrated, as was consistency with the results from a previous 7-day trial that involved two of the formulations (1.2% HEC gel, 2.0% N-9). The 1.0% C31G co-polymer gel was the best tolerated, most acceptable formulation, and will be advanced to longer, more comprehensive trials. Thus, formulation differences are relevant to microbicide tolerance and acceptability, and the 3-day trial design validated in this study can be used to assess formulations.
尽管全球对有效杀微生物剂以减少性传播疾病(STD)和HIV传播有巨大需求,但目前尚无可用产品。C31G是一种表面活性抗感染剂,在体外对细菌性和病毒性STD病原体具有活性,在一项为期3天、每日给药一次的临床试验中进行了评估,该试验旨在评估多种制剂的安全性和可接受性。该试验使用了一种评分算法,该算法基于相关受试者报告的症状以及随访时观察到的体征。结果表明,各制剂之间在耐受性和可接受性方面存在差异,这与之前一项涉及其中两种制剂(1.2%羟乙基纤维素凝胶、2.0%壬苯醇醚-9)的7天试验结果一致。1.0% C31G共聚物凝胶是耐受性最佳、最可接受的制剂,并将推进到更长、更全面的试验。因此,制剂差异与杀微生物剂的耐受性和可接受性相关,本研究中验证的3天试验设计可用于评估制剂。