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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
Jun 19, 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, evaluates the immunogenicity superiority of booster doses with Omicron and trivalent vaccines compared to the CoronaVac vaccine in a previously vaccinated adult population in Chile. Given the ongoing global demand for effective COVID-19 vaccines, particularly against emerging variants, this study could position the Omicron and trivalent vaccines favorably in the competitive landscape. The results may enhance the commercial viability of these vaccines, especially if they demonstrate superior immunogenicity, potentially leading to expanded market opportunities and partnerships, particularly with Sinovac Life Sciences Co., Ltd. Furthermore, the trial's completion and subsequent data could attract interest from investors and stakeholders focused on pandemic preparedness and vaccine development.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05593042
Indication
COVID-19
Modality
vaccine
Target
SARS-CoV-2 virus (Omicron variant and ancestral strains) through humoral immunogenicity.
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.