Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Flucelvax QIV is a cell-culture-derived quadrivalent inactivated subunit influenza vaccine developed by Seqirus (a CSL company). Unlike traditional influenza vaccines produced in embryonated chicken eggs, Flucelvax QIV is manufactured using Madin-Darby Canine Kidney (MDCK) cells. This cell-based production method avoids egg-adaptive mutations that can occur during viral propagation in eggs, potentially leading to a closer match between the vaccine antigens and circulating wild-type viruses. The vaccine contains purified haemagglutinin (HA) antigens from four influenza virus strains (two influenza A subtypes and two influenza B lineages) as recommended by the World Health Organization. It is indicated for the prevention of seasonal influenza in adults and children. Clinical evaluations, such as the ComFluCOV trial, have also assessed its safety and immunogenicity when co-administered with COVID-19 vaccines.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Flucelvax QIV.