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NCT05593042COMPLETEDanonymous

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

Sponsor

Source record

Pontificia Universidad Catolica de Chile

Phase

Source record

Phase 2

Modality

AI-normalized

vaccine

Target

AI-normalized

SARS-CoV-2 virus (Omicron variant and ancestral strains) through humoral immunogenicity.

Indication / condition

AI-normalized

COVID-19

Intervention

Source record

CoronaVac®, Omicron Vaccine, Trivalent Vaccine

Source & freshness

Source record

NCT ID

NCT05593042

Original source

ClinicalTrials.gov

Source last updated

Feb 07, 2024

Ingested at

Jun 19, 2026

Internal sync

Jun 19, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT05593042

Title

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

Sponsor

Pontificia Universidad Catolica de Chile

Status

COMPLETED

Phase

Phase 2

Condition raw

COVID-19, Vaccines

Condition normalized

COVID-19, Vaccines

Modality raw

vaccine

Modality normalized

vaccine

Target raw

SARS-CoV-2 virus (Omicron variant and ancestral strains) through humoral immunogenicity.

Target normalized

SARS-CoV-2 virus (Omicron variant and ancestral strains) through humoral immunogenicity.

Interventions

CoronaVac®, Omicron Vaccine, Trivalent Vaccine

Public preview

Source record

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.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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