Microbicides - evaluating multiple formulations of C31G

被引:38
作者
Bax, R
Douville, K
McCormick, D
Rosenberg, M
Higgins, J
Bowden, M
机构
[1] Biosyn Inc, Huntingdon Valley, PA 19006 USA
[2] Hlth Decis Ltd, Chapel Hill, NC 27514 USA
关键词
microbicide; C31G; STD; clinical trial;
D O I
10.1016/S0010-7824(02)00389-X
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
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. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:365 / 368
页数:4
相关论文
共 9 条
  • [1] Safety of single daily use for one week of C31G HEC gel in women
    Ballagh, SA
    Baker, JM
    Henry, DM
    Archer, DF
    [J]. CONTRACEPTION, 2002, 66 (05) : 369 - 375
  • [2] Heterosexual transmission of HIV in Haiti
    Deschamps, MM
    Pape, JW
    Hafner, A
    Johnson, WD
    [J]. ANNALS OF INTERNAL MEDICINE, 1996, 125 (04) : 324 - 330
  • [3] Inactivation of human immunodeficiency virus type 1 by nonoxynol-9, C31G, or an alkyl sulfate, sodium dodecyl sulfate
    Krebs, FC
    Miller, SR
    Malamud, D
    Howett, MK
    Wigdahl, B
    [J]. ANTIVIRAL RESEARCH, 1999, 43 (03) : 157 - 173
  • [4] MALAMUD D, 1998, FORMULATION C31G VAG, P79
  • [6] SARACCO A, 1993, J ACQ IMMUN DEF SYND, V6, P497
  • [7] Thompson KA, 1996, CONTRACEPTION, V53, P313
  • [8] WYRICK B, 1997, ANTIMICROB AGENTS CH, V4, P1335
  • [9] 2002, SCI MICROBICIDES EXE