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ACTIVE NOT RECRUITING
NCT07812142

Retrospective Analysis of the Second Year of Safety Surveillance of the Qdenga® (TAK-003) Vaccine in Private Vaccination Centers, Including a Sub-analysis of Safety in Adults Over 60 Years of Age

Sponsor: Fundación Vacunar

View on ClinicalTrials.gov

Summary

The TAK-003 vaccine, Qdenga, developed by Takeda, was approved by ANMAT in April 2023 and has been available in Argentina since November 2023 for individuals aged 4 years and older, with no upper age limit. Clinical trials demonstrate that Qdenga has a favorable safety and immunogenicity profile in individuals with and without prior dengue infection. However, real-world safety evidence remains limited, particularly in adults over 60 years of age. The aim of this study is to evaluate adverse events following immunization (AEFI) associated with TAK-003 during the second year of implementation and across the combined two-year period at private vaccination centers in the Buenos Aires metropolitan area, with a particular focus on older adults and hypersensitivity reactions.

Key Details

Gender

All

Age Range

4 Years - Any

Study Type

OBSERVATIONAL

Enrollment

94526

Start Date

2024-11-02

Completion Date

2026-12-01

Last Updated

2026-09-10

Healthy Volunteers

Yes

Conditions

Interventions

BIOLOGICAL

Tak-003

Q- Denga vaccine in population \>4 years without age limit

Locations (1)

Fundación Vacunar

Buenos Aires, Argentina