Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | Dengue 1,2,3,4 (attenuated) vaccine | Dose 1000 PFU per virus (1,2,3,4) Route:subcutaneous |
| OTHER | Placebo | Route: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.