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Yellow Fever Human Infection Model With YF-17D

Yellow Fever Human Infection Model With YF-17D

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05901454
Acronym
YF-INFECT
Enrollment
30
Registered
2023-06-13
Start date
2023-02-17
Completion date
2024-03-01
Last updated
2023-06-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Yellow Fever

Brief summary

No antiviral treatment exists for yellow fever, only supportive care, and therefore we rely on prevention through vaccination. Although this vaccine is very effective, stockpiles are insufficient in outbreak situations and some people have a contraindication to be vaccinated. For those who are unprotected and at risk of yellow fever infection, treatment could be life saving.

Detailed description

No antiviral treatment exists for yellow fever, only supportive care, and therefore we rely on prevention through vaccination. Although this vaccine is very effective, stockpiles are insufficient in outbreak situations and some people have a contraindication to be vaccinated. For those who are unprotected and at risk of yellow fever infection, treatment could be life saving.

Interventions

DRUGYellow Fever Vaccine

vaccination according to manufacturers manual (0.5mL subcutaneously in the arm)

Sponsors

The International Society of Travel Medicine
CollaboratorUNKNOWN
Leiden University Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

human infection model of yellow fever with the yellow fever 17D vaccine and viruria (virus in urine) as readout

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* age 18-50 years

Exclusion criteria

* contraindication to receive YF-17D (immune deficiency, thymus illness) * previous YF vaccination * pregnancy * chicken egg allergy * hypersensitivity to any other substance in the YF-17D vaccine * interval of \< 4 weeks of another live attenuated vaccine

Design outcomes

Primary

MeasureTime frameDescription
yellow fever 17D in urinewithin 30 days of the vaccinationyellow fever 17D in urine at sequential time points after vaccination

Secondary

MeasureTime frameDescription
peak of YF 17D viruria after vaccinationwithin 30 days of the vaccinationdays after vaccination on which most participants have a positive yellow fever virus PCR on urine as material
YF-17D viremia (in plasma) after vaccinationwithin 14 days of the vaccinationdays after vaccination on which most participants have a positive yellow fever virus PCR on plasma as material

Countries

Netherlands

Contacts

Primary ContactAnna H Roukens, MD, PhD
a.h.e.roukens@lumc.nl+31715262613
Backup ContactLeo G Visser, MD PhD
l.g.visser@lumc.nl+31715262613

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026