CompletedPhase 2NCT05142553
Immunogenicity and Safety of a Booster Vaccination With a Recombinant Protein RBD Candidate Vaccine Against SARS-CoV-2 in Healthy Adults Volunteers Fully Vaccinated Followed by an Extension Period to Study a Fourth Dose Administration.
Studying Severe acute respiratory syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Hipra Scientific, S.L.U
- Principal Investigator
- Teresa PratHIPRA SCIENTIFIC
- Intervention
- COVID-19 Vaccine HIPRA(biological)
- Enrollment
- 887 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2021 – 2023
Study locations (10)
- Hospital Germans Trias I Pujol, Badalona, BARCELONA, Spain
- Hospital Vall Hebron, Barcelona, BARCELONA, Spain
- Hospital Clinic de Barcelona, Barcelona, Barcelona, Spain
- Hospital Universitari Dr. Josep Trueta, Girona, Girona, Spain
- Hospital Gregorio Marañón, Madrid, Madrid, Spain
- Hospital Universitario La Paz, Madrid, Madrid, Spain
- Hospital Principe de Asturias, Meco, Madrid, Spain
- Hospital Regional Universitario de Málaga, Málaga, Málaga, Spain
- Hospital Clínico de Valencia, Valencia, Valencia, Spain
- Hospital de Cruces, Barakaldo, VIZCAYA, Spain
Collaborators
Laboratorios Hipra, S.A.
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT05142553 on ClinicalTrials.govOther trials for Severe acute respiratory syndrome
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