Petri Eckhardt, Biswal Shibadas, Lloyd Eric, Tricou Vianney, Folschweiller Nicolas
Takeda Pharmaceuticals International AG, Zurich, Switzerland.
Takeda Vaccines, Inc., Cambridge, MA, USA.
Vaccine. 2024 Dec 2;42(26):126309. doi: 10.1016/j.vaccine.2024.126309. Epub 2024 Sep 7.
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.
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。