TrialSignal
Clinical trial intelligence report
Phase I Clinical Trial to Evaluate the Safety, Tolerability and Preliminary Immunogenicity of SARS-CoV-2 mRNA Vaccine (LVRNA009) in Chinese People Aged 18 Years and Over
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT05364047-Jul 28, 2026
NCT ID
NCT05364047
Status
UNKNOWN
Phase
Phase 1
Sponsor
AIM Vaccine Co., Ltd.
Executive brief
Investment-Ready Snapshot
AIM Vaccine Co., Ltd. is conducting a Phase I clinical trial of the mRNA vaccine LVRNA009 targeting the SARS-CoV-2 virus in the Chinese population aged 18 years and older. The trial aims to assess safety, tolerability, and preliminary immunogenicity. Given the ongoing global demand for effective COVID-19 vaccines, this asset has potential commercial value, particularly in the Chinese market where vaccination efforts continue. The competitive landscape includes established players like Pfizer-BioNTech and Moderna, which may pose challenges in market penetration. Diligence is warranted to evaluate the trial's progress and any emerging data that could influence market positioning.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05364047
Indication
COVID-19
Modality
RNA therapy
Target
SARS-CoV-2 Spike Protein
Intervention
Low-dose of LVRNA009, Middle-dose of LVRNA009, High-dose of LVRNA009, Placebo
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.