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Clinical Trial Summary

Yellow fever is an acute febrile infectious disease transmitted to man urban cycle by mosquitoes infected by an arbovirus of the genus Flavivirus family Flaviviridae. Its occurrence is recorded in South America Central America and Africa. In cities the yellow fever vector is the Aedes aegypti mosquito which also transmits dengue viruses zika and chikungunya. This disease is more frequent in males and the most affected age group is above fifteen years due to the greater exposure related to the penetration in wild areas of the endemic zone of yellow fever. Another risk group is unvaccinated people who live near wild environments where the virus circulates. According to the World Health Organization a single dose of the yellow fever vaccine is sufficient to maintain protective immunity against yellow fever for a lifetime therefore a booster dose is not required. This question is difficult to evaluate because there is no serological correlate of protection against yellow fever and seropositivity is defined with several cut off points. Although studies indicate that the duration of protection after vaccination is long there is considerable evidence in the literature that antibody titer falls over the years reaching levels considered as seronegative in at least a portion of the vaccinees. This is of more concern to people living in endemic areas who are exposed to the virus throughout their lives. For this reason Brazil recommended revaccinating once at least until additional studies were done. The need to increase Bio Manguinhos production capacity to meet the increased demand from Brazil and other countries is urgent. The occurrence of epidemics when millions of individuals need to be vaccinated in a short period of time exceeds production capacity and this is a recurrent problem. The current vaccine has a very high potency well above the thousand international units recommended by World Health Organization. But we need to generate additional evidence that very low doses of viral particles in the yellow fever vaccine are still immunogenic and that their immunogenicity can be maintained for at least ten years after vaccination. This evidence will support the rapid increase of their availability by the fractionation of doses or other alternatives.


Clinical Trial Description

This is an observational study in young adult males who received the first dose of the yellow fever vaccine when they participated in the Dose response study of the yellow fever vaccine produced by Bio Manguinhos Fiocruz. The purpose of this study is to know whether reduced dose immunity is maintained for at least ten years. This information is crucial to support the recommendation to use fractional dose in adults a topic of great interest to World Health Organization. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04416477
Study type Observational
Source The Immunobiological Technology Institute (Bio-Manguinhos) / Oswaldo Cruz Foundation (Fiocruz)
Contact Akira Homma
Phone +55 (21) 3882-9479
Email Akira@bio.fiocruz.br
Status Recruiting
Phase
Start date April 8, 2019
Completion date August 31, 2020

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT01244802 - Characterization of Human Memory Immune Responses to Prior Yellow Fever Vaccination
Completed NCT03116802 - Yellow Fever Vaccine on Statin/ Non Statin Subjects Phase 2
Completed NCT03338231 - Clinical Study of Immunity Duration of Yellow Fever Vaccine in Military N/A
Active, not recruiting NCT03591003 - "Persistence of Neutralizing Antibodies Against Yellow Fever (YF) in HIV-infected Patients"
Active, not recruiting NCT02555072 - Immunity Period After One Dose of Yellow Fever Vaccine in Adults and Children (Paraiba Study) Phase 4