drugset / Trial / NCT05246137
A Phase III Trial to Assess the Safety and Immunogenicity of a HIPRA's Candidate Booster Vaccination Against COVID-19.
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PHH-1V | Vaccine | 40 ug | Intramuscular |