首页> 外文期刊>Journal of postgraduate medicine. >A clinical trial to assess the immunogenicity and safety of Inactivated Influenza Vaccine (Whole Virion) IP (Pandemic Influenza (H1N1) 2009 Monovalent Vaccine; VaxiFlu-S TM ) in healthy Indian adult population
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A clinical trial to assess the immunogenicity and safety of Inactivated Influenza Vaccine (Whole Virion) IP (Pandemic Influenza (H1N1) 2009 Monovalent Vaccine; VaxiFlu-S TM ) in healthy Indian adult population

机译:评估健康印度成年人群中灭活流感疫苗(全病毒颗粒)IP(大流行性流感(H1N1)2009单价疫苗; VaxiFlu-S TM)的免疫原性和安全性的临床试验

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Background : The pandemic of H1N1 2009 influenza has spread world over and low degree of virus transmission has continued in several regions of India. Aims : To assess the immunogenicity and safety of Pandemic Influenza (H1N1) 2009 Monovalent Vaccine in healthy adult Indian population. Settings and Design : Prospective, open label, multicentric, phase 2/3 clinical trial. Materials and Methods : Healthy adult Indian subjects belonging to either 18-59 years or ≥60 years age groups were enrolled and administered a single 0.5 ml (≥15 mcg of hemagglutinin antigen) dose of vaccine in the deltoid muscle. Anti-hemagglutinin antibody titer was assessed at baseline and 21 (±2) days after vaccination by Hemagglutination Inhibition (HI) test. Safety assessments were done for a period of 42 days. Statistical Analysis Used : Percentages of appropriate population with 95% confidence intervals calculated, log transformation of the data to calculate Geometric Mean Titers (GMTs) and chi-square test and student's t-test applied for significance testing. Results : 182/198 and 53/63 volunteers in age groups of 18-59 years and ≥60 years, respectively, achieved an HI titer ≥1 : 40 at Day 21 (91.9% [95% confidence interval: 88.1-95.7%] and 84.1% [75.1-93.2%]; P=0.072). Further, 171/198 and 50/63 volunteers in the respective age groups achieved seroconversion/four-fold increase in titer at Day 21 (86.4% [81.6-91.1%] and 79.4% [69.4-89.4%]; P=0.179). A significant rise of 22.6-fold [18.0-28.4] and 10.5-fold [7.4-15.0] was noted in GMT in the respective age groups (P0.001 for both groups as compared to baseline). Nine vaccine-related adverse events were reported (3.4% incidence [1.2-5.6%]), which were of low severity only. Conclusions : Pandemic Influenza (H1N1) 2009 Monovalent Vaccine produces excellent immunogenic response with a good tolerability profile in adult Indian population.
机译:背景:2009年H1N1流感大流行已蔓延至世界各地,印度几个地区的病毒传播程度仍很低。目的:评估健康成人印度人口中2009年H1N1大流行性流感的免疫原性和安全性。设置和设计:前瞻性,开放标签,多中心,2/3期临床试验。材料和方法:纳入18-59岁或≥60岁年龄组的健康印度成年受试者,并在三角肌中注射0.5 ml(≥15 mcg血凝素抗原)单剂疫苗。通过血凝抑制(HI)试验在接种后的基线和21(±2)天评估抗血凝素抗体滴度。安全评估进行了42天。使用的统计分析:计算出具有95%置信区间的适当总体的百分比,对数据进行对数转换,以计算几何均数滴度(GMT)以及卡方检验和学生t检验用于显着性检验。结果:18-59岁和≥60岁年龄组的182/198和53/63志愿者分别在第21天达到HI滴度≥1:40(91.9%[95%置信区间:88.1-95.7%])和84.1%[75.1-93.2%]; P = 0.072)。此外,各个年龄段的171/198和50/63志愿者在第21天达到血清转化/滴度增加四倍(86.4%[81.6-91.1%]和79.4%[69.4-89.4%]; P = 0.179) 。各个年龄组的格林尼治标准时间(GMT)分别显着上升了22.6倍[18.0-28.4]和10.5倍[7.4-15.0](与基线相比,两组的P <0.001)。据报告有9种疫苗相关的不良事件(发生率3.4%[1.2-5.6%]),严重程度仅次于低级。结论:2009年大流行性流感(H1N1)单价疫苗在印度成年人群中产生了出色的免疫原性反应,并具有良好的耐受性。

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