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TAK-003登革热疫苗的早期保护作用:来自DEN-301临床试验的数据。

Early onset of protection of the TAK-003 dengue vaccine: Data from the DEN-301 clinical trial.

作者信息

Petri Eckhardt, Biswal Shibadas, Lloyd Eric, Tricou Vianney, Folschweiller Nicolas

机构信息

Takeda Pharmaceuticals International AG, Zurich, Switzerland.

Takeda Vaccines, Inc., Cambridge, MA, USA.

出版信息

Vaccine. 2024 Dec 2;42(26):126309. doi: 10.1016/j.vaccine.2024.126309. Epub 2024 Sep 7.

Abstract

Exploring time-to-onset of efficacy of the live-attenuated dengue vaccine TAK-003 is important for individuals living in, or traveling to, dengue-endemic areas. This protocol-defined exploratory analysis of the Tetravalent Immunization against Dengue Efficacy Study (TIDES) investigated TAK-003's onset of efficacy after the first and before the second dose, administered 3 months later, in healthy participants aged 4-16 years randomly assigned 2:1 to receive TAK-003 or placebo. The number of virologically confirmed dengue (VCD) cases between first and second vaccinations and the time-to-onset of vaccine efficacy (VE) were assessed in the safety population. Fifty VCD cases occurred between the first and second doses (placebo = 37, TAK-003 = 13). The VE against VCD up to 3 months after the first dose was 82.1 %, with an estimated time-to-onset of ∼14 days. TAK-003 provides rapid onset of protection after the first dose and may be useful in the context of a dengue outbreak or as a travel vaccine.

摘要

对于生活在登革热流行地区或前往该地区旅行的人来说,探索减毒活登革热疫苗TAK-003的起效时间很重要。本方案定义的登革热四价免疫效力研究(TIDES)探索性分析,调查了在4至16岁健康参与者中,TAK-003在首剂接种后且在3个月后接种第二剂之前的起效情况,这些参与者按2:1随机分配接受TAK-003或安慰剂。在安全性人群中评估了首剂和第二剂接种之间病毒学确诊的登革热(VCD)病例数以及疫苗效力(VE)的起效时间。首剂和第二剂之间发生了50例VCD病例(安慰剂组 = 37例,TAK-003组 = 13例)。首剂接种后长达3个月的VCD VE为82.1%,估计起效时间约为14天。TAK-003在首剂接种后能迅速提供保护,在登革热暴发情况下或作为旅行疫苗可能有用。

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