drugset / Trial / NCT05305573

Assessing the Immunogenicity and Safety of a HIPRA's Candidate Booster Vaccination in Adults Fully Vaccinated With Adenovirus Vaccine Against COVID-19.

NCT05305573

Phase 2 Completed 26 enrolled Hipra Scientific, S.L.U
RandomizedParallel-groupDouble-blindPrevention

Summary

Phase IIb clinical trial to assess the Immunogenicity and Safety of a HIPRA's Candidate Booster vaccination (PHH-1V) in adults fully vaccinated with the adenovirus vaccine Vaxevria against COVID-19.

Timeline

Start
2022-03-25
Primary completion
2022-10-01
Completion
2022-10-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator BNT162b2 Messenger RNA (mRNA) 30 ug
Subject PHH-1V Vaccine 40 ug

Indications