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A Randomized, Blinded and Placebo-Control Phase I Clinical Trial to Evaluate the Safety and Immunogenicity of Lyophilized Respiratory Syncytial Virus mRNA Vaccine in Adults Aged 18 Years or Above
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT07289503-Jul 28, 2026
NCT ID
NCT07289503
Status
ACTIVE_NOT_RECRUITING
Phase
Phase 1
Sponsor
Suzhou Abogen Biosciences Co., Ltd.
Executive brief
Investment-Ready Snapshot
Suzhou Abogen Biosciences Co., Ltd. is advancing its mRNA vaccine candidate ABO1105 for Respiratory Syncytial Virus (RSV) through a Phase 1 clinical trial. The trial aims to assess the safety and immunogenicity of the vaccine in healthy adults aged 18 years and older. Given the increasing incidence of RSV infections and the lack of effective vaccines on the market, this asset has significant commercial potential. The competitive landscape includes other mRNA-based vaccines and traditional vaccine approaches, but Abogen's focus on a lyophilized formulation may offer logistical advantages. The trial's outcomes could position Abogen favorably in the growing vaccine market, particularly as RSV is a major cause of respiratory illness in infants and the elderly. Diligence should focus on regulatory pathways, potential partnerships, and market entry strategies post-trial completion.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT07289503
Indication
Respiratory Syncytial Virus
Modality
protein therapy
Target
Respiratory Syncytial Virus (RSV)
Intervention
ABO1105, 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.