ClinConnect ClinConnect Logo
Search / Trial NCT03927131

Safety and Immunogenicity of the Butantan Quadrivalent Influenza Vaccine

Launched by BUTANTAN INSTITUTE · Apr 23, 2019

Trial Information

Current as of May 22, 2025

Completed

Keywords

Vaccines

ClinConnect Summary

This is a double blinded, randomized active-control comparator study to assess the safety and immunogenicity of QIV-IB, the Butantan Institute quadrivalent influenza vaccine candidate. As active controls, two trivalent influenza vaccines with different Influenza B strains, one with influenza B/Victoria strain (TIVV-IB) and other with influenza B/Yamagata strain (TIVY-IB).

The study is designed to build a safety database of the quadrivalent influenza vaccine in adults to detect adverse events with a frequency of 1:1000 or higher and safety databases for elderly and pediatric age groups to d...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Male or female, age 3 years or older at the time of enrollment.
  • Provide written informed consent
  • Agrees to complete all study visits, procedures and contacts
  • Women and adolescents of childbearing age: Negative pregnancy test with understanding (through informed consent process).
  • Exclusion Criteria:
  • Chronic medical conditions such as psychiatric conditions, diabetes, hypertension or any other conditions that might place the subjects at high risk of adverse events. Study clinicians will use clinical judgment on a case-by-case basis to assess safety risks under this criterion.
  • Clinically significant abnormalities on physical examination.
  • Use of immunosuppressive medications such as systemic corticosteroids or chemotherapeutics, or immunosuppressive illness.
  • Women who are pregnant or planning to become pregnant during the study period plus 3 months beyond the last vaccine dose and currently nursing women.
  • Participation in research involving another investigational product within 30 days before planned date of first vaccination or anytime through the last study safety visit.
  • Clinically significant abnormalities on basic laboratory screening tests.
  • Acute febrile illness (axillar temperature ≥ 37.8°C)
  • Hypersensitivity to egg or chicken proteins or any of the vaccine constituents
  • Thrombocytopenia or a bleeding disorder contraindicating intramuscular vaccination
  • Unstable chronic illness (defined as illness requiring hospitalization or a clinically significant change in medication in the previous 12 weeks).
  • Alcohol abuse of alcohol or drug addiction
  • Any vaccination within the previous 4 weeks
  • Seasonal influenza vaccination in the current year

About Butantan Institute

The Butantan Institute is a renowned biomedical research center based in São Paulo, Brazil, dedicated to the development of vaccines and biopharmaceuticals. Established in 1901, it has become a key player in public health initiatives, focusing on the prevention and treatment of infectious diseases. With a commitment to scientific excellence, the Institute engages in extensive clinical trials to evaluate the safety and efficacy of its products, contributing significantly to global health advancements. Its state-of-the-art facilities and collaboration with international research communities underscore its role as a leader in immunological research and vaccine production.

Locations

Fortaleza, Ceará, Brazil

Belo Horizonte, Minas Gerais, Brazil

Recife, Pernambuco, Brazil

Pelotas, Rio Grande Do Sul, Brazil

Porto Alegre, Rio Grande Do Sul, Brazil

Laranjeiras, Sergipe, Brazil

Ribeirão Preto, São Paulo, Brazil

Serrana, São Paulo, Brazil

São Caetano Do Sul, São Paulo, Brazil

São José Do Rio Preto, São Paulo, Brazil

São Paulo, , Brazil

Fortaleza, Ceará, Brazil

Patients applied

0 patients applied

Trial Officials

Fernanda Castro Boulos, MD

Study Director

Instituto Butantan

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials