drugset / Trial / NCT05246137

A Phase III Trial to Assess the Safety and Immunogenicity of a HIPRA's Candidate Booster Vaccination Against COVID-19.

NCT05246137

Phase 3 Completed 2646 enrolled Hipra Scientific, S.L.U
NaSingle-groupOpen-labelPrevention

Summary

This is a phase III clinical study to assess the safety, tolerability and immunogenicity of PHH-1V as a booster dose in healthy adult subjects vaccinated against COVID-19 with the Comirnaty, Spikevax, Vaxevria or Janssen vaccine.

Timeline

Start
2022-02-03
Primary completion
2022-03-03
Completion
2023-03-03

Drugs

EvaluationDrugModalityDoseRoute
Subject PHH-1V Vaccine 40 ug Intramuscular

Indications