Drug intelligence / Profile preview

H7N9 antigen + adjuvant SE

Development stage
Unknown
Lead developer
Sanofi Pasteur
Modality
Nanoparticles → Drug Delivery Systems, Recombinant Proteins and Enzymes, Vaccines & Immunotherapeutics
Administration
Intramuscular
01

Overview

H7N9 antigen + adjuvant SE is a combination pandemic influenza vaccine candidate composed of an inactivated split-virus hemagglutinin (HA) antigen derived from the A/Shanghai/2/2013(H7N9) strain and formulated with the squalene-based oil-in-water emulsion adjuvant known as "SE" (manufactured by Infectious Disease Research Institute, IDRI). The addition of the SE adjuvant enhances immunogenicity, enabling dose-sparing by eliciting stronger antibody responses at lower HA doses compared to non-adjuvanted formulations. This approach aims to improve pandemic preparedness by increasing immune response efficiency and expanding available vaccine supply. Clinical studies have shown that vaccines using this formulation are safe and well-tolerated, though local reactogenicity (injection site pain) is more common than in non-adjuvanted vaccines. The primary indication is prevention of infection caused by avian influenza A(H7N9)[4].

Other names
H7N9 vaccine with SEH-7N9 vaccine with SEH 7N9 vaccine with SEH7N9 split-virus vaccine with SE adjuvantH-7N9 split-virus vaccine with SE adjuvantH 7N9 split-virus vaccine with SE adjuvant
02

Targets

BCR (Immunoglobulin G B Cell Receptor)T-cell receptor recognizing H7N9 hemagglutinin-derived peptide–MHC complexes

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