Kulkarni Prasad S, Desai Sajjad, Tewari Tushar, Kawade Anand, Goyal Nidhi, Garg Bishan Swarup, Kumar Dinesh, Kanungo Suman, Kamat Veena, Kang Gagandeep, Bavdekar Ashish, Babji Sudhir, Juvekar Sanjay, Manna Byomkesh, Dutta Shanta, Angurana Rama, Dewan Deepika, Dharmadhikari Abhijeet, Zade Jagdish K, Dhere Rajeev M, Fix Alan, Power Maureen, Uprety Vidyasagar, Parulekar Varsha, Cho Iksung, Chandola Temsunaro R, Kedia Vikash K, Raut Abhishek, Flores Jorge
Serum Institute of India Pvt Ltd, Pune, India.
Serum Institute of India Pvt Ltd, Pune, India.
Vaccine. 2017 Oct 27;35(45):6228-6237. doi: 10.1016/j.vaccine.2017.09.014. Epub 2017 Sep 26.
Rotavirus is the most common cause of moderate-to-severe infant diarrhoea in developing countries, resulting in enormous morbidity, mortality, and economic burden. A bovine-human reassortant pentavalent rotavirus vaccine (BRV-PV) targeting the globally most common strains was developed in India and tested in a randomized, double-blind, placebo-controlled end-point driven Phase III efficacy clinical trial implemented at six sites across India. Infants 6 to 8weeks of age were randomized (1:1) to receive three oral doses of BRV-PV or placebo at 6, 10, and 14weeks of age along with routine vaccines. Home visit surveillance was conducted to detect severe rotavirus gastroenteritis (SRVGE) and safety outcomes until the children reached two years of age. A total of 3749 infants received BRV-PV while 3751 received placebo. At the time of the primary end-point (when the minimum number of cases needed for analysis were accrued) the vaccine efficacy against SRVGE was 36% (95% CI 11.7, 53.6, p=0.0067) in the per protocol (PP) analysis, and 41.9% (95% CI 21.1, 57.3, p=0.0005) in the intent to treat (ITT) analysis. Vaccine efficacy over the entire follow-up period (until children reached two years of age) was 39.5% (95% CI 26.7, 50, p<0.0001) in the PP analysis and 38.8% (95% CI, 26.4, 49, p<0.0001) in the ITT analysis. Vaccine efficacy against the very severe rotavirus cases (VSRVGE, Vesikari score≥16) was 60.5% (95% CI 17.7, 81, p=0.0131) at the time of the primary analysis and 54.7% (95% CI 29.7, 70.8, p=0.0004) for the complete follow-period in the PP population. The incidence of solicited, unsolicited, and serious adverse events were similar in both the vaccine and placebo groups. Likewise, the number of intussusceptions and deaths were similar between both groups. Thus, BRV-PV is an effective, well tolerated and safe vaccine in Indian infants. (Trial registration: Clinical Trials.Gov [NCT 02133690] and Clinical Trial Registry of India [CTRI/2013/05/003667]).
轮状病毒是发展中国家中度至重度婴幼儿腹泻的最常见病因,会导致巨大的发病率、死亡率和经济负担。一种针对全球最常见毒株的牛 - 人重配五价轮状病毒疫苗(BRV - PV)在印度研发,并在印度六个地点开展的一项随机、双盲、安慰剂对照、终点驱动的III期疗效临床试验中进行了测试。6至8周龄的婴儿被随机分组(1:1),在6、10和14周龄时与常规疫苗一起口服三剂BRV - PV或安慰剂。进行家访监测以检测严重轮状病毒胃肠炎(SRVGE)和安全性结局,直至儿童满两岁。共有3749名婴儿接受了BRV - PV,3751名接受了安慰剂。在主要终点时(当积累了分析所需的最少病例数时),按方案(PP)分析中,疫苗对SRVGE的效力为36%(95%CI 11.7, 53.6,p = 0.0067),在意向性分析(ITT)中为41.9%(95%CI 21.1, 57.3,p = 0.0005)。在整个随访期(直至儿童满两岁),PP分析中疫苗效力为39.5%(95%CI 26.7, 50,p<0.0001),ITT分析中为38.8%(95%CI 26.4, 49,p<0.0001)。在主要分析时,疫苗对非常严重的轮状病毒病例(VSRVGE,Vesikari评分≥16)的效力为60.5%(95%CI 17.7, 81,p = 0.0131),在PP人群的整个随访期为54.7%(95%CI 29.7, 70.8,p = 0.0004)。疫苗组和安慰剂组中诱发、非诱发和严重不良事件的发生率相似。同样,两组之间肠套叠和死亡的数量也相似。因此,BRV - PV在印度婴儿中是一种有效、耐受性良好且安全的疫苗。(试验注册:ClinicalTrials.Gov [NCT 02133690] 和印度临床试验注册中心 [CTRI/2013/05/003667])