Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The combination of a cell-culture trivalent influenza vaccine (cTIV) and a 23-valent pneumococcal polysaccharide vaccine (PPSV23) refers to the co-administration of two distinct vaccines to provide simultaneous protection against seasonal influenza and pneumococcal disease. The cTIV component, such as Flucelvax, is manufactured using mammalian cell culture technology (typically MDCK cells) rather than traditional egg-based methods, which reduces the risk of egg-adaptive mutations that can decrease vaccine effectiveness. It contains hemagglutinin from three influenza strains: two Influenza A subtypes (H1N1 and H3N2) and one Influenza B lineage. The PPSV23 component, such as Pneumovax 23, contains purified capsular polysaccharides from 23 serotypes of *Streptococcus pneumoniae*, which are responsible for the majority of invasive pneumococcal infections. This co-administration strategy is primarily utilized in elderly populations (65 years and older) and high-risk individuals to improve vaccination coverage and provide broad immunity against respiratory pathogens during the winter season.
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 cell-culture trivalent influenza vaccine + 23-valent pneumococcal polysaccharide vaccine.