drugset / Trial / NCT03525210

Study of Safety, Tolerability and Immunogenicity of Gardasil®9 in Immunocompromised Patients

NCT03525210

Phase 3 Completed 271 enrolled Universitaire Ziekenhuizen KU Leuven
Non-randomizedParallel-groupOpen-labelPrevention

Summary

Patients with immunodeficiencies are at increased risk of developing persistent HPV infection and as such HPV-related disease (genital warts and cancer). In this study HIV-patients and SOT-patients will receive 3 doses of Gardasil®9. Safety, tolerability and immunogenicity will be evaluated up to one month following the 3rd and last dose of Gardasil®9.

Timeline

Start
2018-04-04
Primary completion
2019-09-01
Completion
2020-07-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Gardasil 9 Vaccine