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Phase 2, Randomized, Double-blind Study to Evaluate Immunogenicity Superiority of a Booster Dose With an Omicron or a Trivalent Vaccine Compared to CoronaVac, in Adults Immunized With Different Vaccine Schedules Against SARS-CoV-2 in Chile
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Aug 04, 2026
Report code
NCT05593042-Aug 04, 2026
NCT ID
NCT05593042
Status
COMPLETED
Phase
Phase 2
Sponsor
Pontificia Universidad Catolica de Chile
Executive brief
Investment-Ready Snapshot
The Phase 2 clinical trial, sponsored by Pontificia Universidad Catolica de Chile, aims to evaluate the immunogenicity superiority of booster doses with Omicron and trivalent vaccines compared to the CoronaVac vaccine in a population previously vaccinated against SARS-CoV-2. Given the ongoing need for effective COVID-19 vaccines, particularly against emerging variants, this trial addresses a significant market demand. The results could position the Omicron and trivalent vaccines favorably against existing competitors, particularly in regions with high CoronaVac usage. The trial's completion in October 2023 allows for timely data analysis and potential market entry, contingent on favorable outcomes. The collaboration with Sinovac Life Sciences Co., Ltd. suggests a strategic partnership that may enhance distribution and commercialization efforts.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05593042
Indication
COVID-19
Modality
vaccine
Target
SARS-CoV-2 virus (CZ02 strain, ancestral, Delta, and Omicron variants)
Intervention
CoronaVac®, Omicron Vaccine, Trivalent Vaccine
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.