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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 20, 2026
NCT ID
NCT05593042
Status
COMPLETED
Phase
Phase 2
Sponsor
Pontificia Universidad Catolica de Chile
Executive brief
Investment-Ready Snapshot
The Phase 2 trial conducted by Pontificia Universidad Catolica de Chile aims to evaluate the immunogenicity superiority of booster doses with Omicron and trivalent vaccines compared to CoronaVac in adults previously vaccinated against SARS-CoV-2. Given the ongoing need for effective COVID-19 vaccines, particularly against emerging variants, the results of this trial could significantly impact market dynamics and competitive positioning for vaccine developers. The trial's completion in October 2023 positions it well for potential regulatory submissions and market entry, especially in regions with high CoronaVac usage. Collaboration with Sinovac Life Sciences Co., Ltd. may enhance commercial prospects, leveraging established distribution channels and brand recognition.
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 and cellular immune response.
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.