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项与 Anti-CS17 Bovin IgG(Johns Hopkins Bloomberg School of Public Health) 相关的临床试验Protective Efficacy of Orally Delivered Bovine Immunoglobulin, Specific for CS17 Fimbriae and CS17 Minor Fimbrial Adhesin CsbD Against Challenge With a CS17 Strain of Enterotoxigenic Escherichia Coli (ETEC)
This is a Phase II, randomized, double-blind, placebo-controlled study designed to investigate whether hyperimmune bovine milk IgG products specific for CsbD and CS17, protect subjects against diarrhea upon challenge with a CS-17-ETEC strain LSN03-016011/A. The study will also evaluate safety and tolerability of these bovine milk IgG products and describe the immune responses following challenge.
The primary study objectives are: 1) Assess safety of the anti-CsbD and anti-CS17 bovine milk IgG among healthy adult volunteers when orally administered three times a day over 7 days. 2) Determine efficacy of the anti-CsbD bovine milk IgG preparation against ETEC diarrhea upon challenge with CS17-ETEC, and 3)Determine efficacy of the anti-CS17 bovine milk IgG preparation against ETEC diarrhea upon challenge with CS17-ETEC. A secondary objective is to determine efficacy of the anti-CsbD and anti-CS17 bovine milk IgG preparations against moderate to severe ETEC diarrhea upon challenge with CS17-ETEC.
100 项与 Anti-CS17 Bovin IgG(Johns Hopkins Bloomberg School of Public Health) 相关的临床结果
100 项与 Anti-CS17 Bovin IgG(Johns Hopkins Bloomberg School of Public Health) 相关的转化医学
100 项与 Anti-CS17 Bovin IgG(Johns Hopkins Bloomberg School of Public Health) 相关的专利(医药)
100 项与 Anti-CS17 Bovin IgG(Johns Hopkins Bloomberg School of Public Health) 相关的药物交易