Clinical trial

Efficacy, Safety and Immunogenicity of Takeda's Tetravalent Dengue Vaccine (TDV)…

NCT02747927 · Takeda, Industry · Completed

Key facts

NCT number NCT02747927
Title Efficacy, Safety and Immunogenicity of Takeda's Tetravalent Dengue Vaccine (TDV) in Healthy Children
Official title 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
Acronym TIDES
Lead sponsor Takeda, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Healthy Volunteers
Intervention type Biological, Drug
Interventions Placebo, Tetravalent Dengue Vaccine (TDV)
Enrollment 20,099
Start date Apr 26, 2016
Primary completion Jul 11, 2018
Completion Jun 28, 2024
First posted Apr 22, 2016
Last update posted Nov 19, 2025
Countries Brazil, Colombia, Dominican Republic, Nicaragua, Panama, Philippines, Sri Lanka, Thailand

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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