drugset / Trial / NCT05374317

Study of the Safety and Immunogenicity of Reduced Doses of the US Yellow Fever Vaccine

NCT05374317

RandomizedSequentialOpen-labelHealth-services research

Summary

This is an open-label, randomized, exploratory study to evaluate the human immune response to reduced subcutaneous (SQ) dosing of Yellow Fever vaccine compared to the standard FDA approved subcutaneous vaccination dose. The current dose of the US FDA licensed Yellow Fever vaccine is approximately 55,000 plaque-forming unit(s) (PFU) in 0.5 mL administered SQ. Using the licensed dosage as standard, investigators are evaluating reduced doses of 1/5th (0.10 mL) and 1/10th (0.05 mL) standard Yellow Fever vaccine (YF-VAX).

Timeline

Start
2021-06-07
Primary completion
2022-11-02
Completion
2022-11-02

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Yellow Fever Vaccine Vaccine 0.05 ml Subcutaneous
Subject Yellow Fever Vaccine Vaccine 0.1 ml Subcutaneous
Subject Yellow Fever Vaccine Vaccine 0.5 ml Subcutaneous

Indications