Evidence map›Paper›PMID 39173075›Full record

Trial reportPLoS neglected tropical diseases2024

Role of the dengue vaccine TAK-003 in an outbreak response: Modeling the Sri Lanka experience.

LakKumar Fernando, Randee Kastner, Pujitha Wickramasinghe, Asvini D Fernando, Dulanie Gunasekera, Van Hung Nguyen, Mengya Liu, Inge LeFevre, Derek Wallace, Nicolas Folschweiller and 1 more

Registry-linked trialAbstract readClinical Trial
In one paragraph

Trial report in PLoS neglected tropical diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02747927 (Phase III, Double-Blind, Randomized, Placebo-Controlled Trial to Investigate the Efficacy, Safety and Immunogenicity of a Tetravalent Dengue Vaccine), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02747927 phase3completednot on this map

Phase III, Double-Blind, Randomized, Placebo-Controlled Trial to Investigate the Efficacy, Safety and Immunogenicity of a Tetravalent Dengue Vaccine (TDV) Administered Subcutaneously in Healthy Children Aged 4 - 16 Years Old

TypeinterventionalSponsorTakedaRan2016 to 2024Enrolled20,099ConditionsHealthy VolunteersArmsPlacebo, Tetravalent Dengue Vaccine (TDV)
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Mapping climate change-driven epidemics.Frontiers in epidemiology · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

LakKumar FernandoCentre for Clinical Management of Dengue & Dengue Haemorrhagic Fever, Negombo General Hospital, Negombo, Sri Lanka.
Randee KastnerTakeda Vaccines, Inc., Boston, Massachusetts, United States of America.ORCID 0000-0003-3682-3255
Pujitha WickramasingheUniversity of Colombo, Colombo, Sri Lanka.
Asvini D FernandoFaculty of Medicine, University of Kelaniya, Kelaniya, Sri Lanka.
Dulanie GunasekeraFaculty of Medical Sciences, University of Sri Jayawardenenpura, Colombo, Sri Lanka.
Van Hung NguyenVHN Consulting, Montreal, Quebec, Canada.
Mengya LiuTakeda Vaccines, Inc., Boston, Massachusetts, United States of America.
Inge LeFevreTakeda Pharmaceuticals International AG, Zurich, Switzerland.
Derek WallaceTakeda Vaccines, Inc., Boston, Massachusetts, United States of America.
Nicolas FolschweillerTakeda Pharmaceuticals International AG, Zurich, Switzerland.
Shibadas BiswalTakeda Vaccines, Inc., Boston, Massachusetts, United States of America.

Funding

Takeda Vaccines Inc., Cambridge, MA, USA.
6 · The paper itself

Abstract

backgroundOutbreaks of dengue can overburden hospital systems, drastically reducing capacity for other care. The 2017 dengue serotype 2 (DENV-2) outbreak in Sri Lanka coincided with vaccination in an ongoing phase 3 efficacy trial of a tetravalent dengue vaccine, TAK-003 (NCT02747927). Here, we present data on the efficacy of TAK-003 following two doses of the vaccine administered 3 months apart in participants aged 4-16 years in Sri Lanka. In addition, we have used the 2017 outbreak dynamics to model the potential impact of TAK-003 on virologically confirmed dengue (VCD) cases and hospitalizations during an outbreak situation. METHODOLOGY/PRINCIPAL

findingsModeling was performed using an age-structured, host-vector, spatial and stochastic transmission model, assuming 65% vaccine coverage and 30 days until initiation of vaccination. Efficacy of TAK-003 against VCD and hospitalized VCD cases was based on data against DENV-2 from the first year of the phase 3 trial. Vaccine efficacy and safety findings in Sri Lanka were in line with those of the overall trial population. The efficacy estimates in Sri Lanka up to the first 12 months after the second dose of TAK-003 were 94.7% and 95.7% against VCD and hospitalized VCD cases, respectively. Modeling of the trial data over an extended geographic area showed a substantial reduction in cases and a flattening of outbreak curves from TAK-003 use. The baseline vaccination scenario (initiation at 30 days, 65% target coverage, vaccine effective at 14 days, 70% hospitalization rate, VE of 95% for VCD and 97% for hospitalized VCD, and 47% for asymptomatic) resulted in a 69.1% reduction in VCD cases and 72.7% reduction in VCD hospitalizations compared with no vaccination. An extreme high scenario (vaccination initiated at Day 15, 80% coverage rate, baseline VE) resulted in 80.3% and 82.3% reduction in VCD and VCD hospitalizations, respectively. Vaccine performance, speed of vaccination campaign initiation, and vaccine coverage were key drivers in reducing VCD cases and hospitalizations. CONCLUSIONS/SIGNIFICANCE: Overall, the study and modeling results indicate that TAK-003 has the potential of meaningful utility in dengue outbreaks in endemic areas.

Indexed as

DengueDengue VaccinesDisease OutbreaksAdolescentChildChild, PreschoolDengue VirusFemaleHospitalizationHumansMaleSri LankaVaccinationVaccine EfficacyDengue Vaccines

Identifiers

PMID39173075
PMCPMC11419351

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.