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Completed
NCT06898775
Passive Safety Surveillance Data of Dengue Vaccine, Qdenga (TAK 003) in Private Vaccination Sites in Buenos Aires, Argentina.
Conditions: Dengue Vaccines
Sex: All
Ages: 4 Years – N/A
Healthy volunteers: Yes
Enrollment: 112345
Sponsor: Fundación Vacunar
Location: Fundación Vacunar Buenos Aires
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 from 4 years old and without limit of age. Clinical trials demonstrate that Qdenga has a favorable safety profile, adequate immunogenicity for all four serotypes, and efficacy in preventing severe dengue in seropositive and seronegative subjects. However, there are currently limited real-world safety studies on TAK-003, particularly for adults over 60 years old.
The aim of this study is to evaluate Adverse Events Supposedly Attributed to Vaccination and Immunization (AEFI) for TAK-003 vaccine in vaccinated people at private vaccination centers in Buenos Aires metropolitan area.
Eligibility Criteria
Inclusion Criteria:
* All individuals who were vaccinated with Qdenga at Vacunar centers since November 2023 still 1st November 2024, from 4 years of age with no upper limit in accordance with ANMAT approval and for whom safety data is available through the Vacunar centers passive surveillance systems.
Exclusion Criteria:
* Reports with insufficient information to characterize the AEFI will be excluded from the analysis.
Source: ClinicalTrials.gov (NCT06898775). StuddyBuddy aggregates publicly available trial information.