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UnknownNCT02406729

Phase III Trial to Evaluate Efficacy and Safety of a Tetravalent Dengue Vaccine

Phase III, Double-Blind, Randomized, Placebo-Controlled Trial to Evaluate the Efficacy, Safety, and Immunogenicity of the Dengue 1, 2, 3, 4 (Attenuated) Vaccine From Instituto Butantan

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
16,935 (estimated)
Sponsor
Butantan Institute · Other Government
Sex
All
Age
24 Months – 59 Years
Healthy volunteers
Accepted

Summary

This is a randomized, multicenter, double-blind, placebo-controlled Phase III study that will evaluate efficacy and safety of a live attenuated, tetravalent, lyophilized dengue vaccine produced by Butantan Institute. The study will be carried out in multiple sites in Brazil. The study will be community-based in select urban areas where there's dengue transmission. Study's intervention will be a single dose of the tetravalent dengue vaccine or placebo in a ratio 2:1. For efficacy analysis will be considered all dengue cases occurring after 28 days post-vaccination in the entire population of 16944 participants. For safety analysis participants will be divided in three age groups: 18 to 59 ys, 7-17 ys and 2 to 6 ys. In each of these age groups there will be a minimum of 4992 participants. The age groups of 18 to 59 ys and 7 to 17 ys will start first. Once safety data for the first 21 days after vaccination is analysed for 450 participants in 7-to17-ys age group, the following group, of 2 to 6 ys, will start. The study's hypothesis is that the vaccine under investigation and produced by Butantan Institute is safe and provides protection against dengue symptomatic disease of 80% or more with a lower bound of the 95% confidence interval of 25%. This way, the expected number of dengue cases virologically confirmed is 24 or more which will provide a response in terms of vaccine efficacy. All participants will be followed up for five years to verify dengue incidence, regardless severity.

Conditions

Interventions

TypeNameDescription
BIOLOGICALDengue 1,2,3,4 (attenuated) vaccineDose 1000 PFU per virus (1,2,3,4) Route:subcutaneous
OTHERPlaceboRoute:subcutaneous

Timeline

Start date
2016-02-22
Primary completion
2021-07-13
Completion
2024-11-01
First posted
2015-04-02
Last updated
2024-02-15

Locations

17 sites across 1 country: Brazil

Source: ClinicalTrials.gov record NCT02406729. Inclusion in this directory is not an endorsement.