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
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.
Indication: Respiratory Syncytial Virus
Modality: protein therapy
Target: Respiratory Syncytial Virus (RSV)
Sponsor: Suzhou Abogen Biosciences Co., Ltd.
Source URL: ClinicalTrials.gov
Source updated: Detailed source ingestion pending
Ingested: Jul 09, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: Respiratory Syncytial Virus (RSV)
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Condition raw: Respiratory Syncytial Virus
Condition normalized: Respiratory Syncytial Virus
Modality raw: protein therapy
Modality normalized: protein therapy
Target raw: Respiratory Syncytial Virus (RSV)
Target normalized: Respiratory Syncytial Virus (RSV)