Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The human papillomavirus type 33 L1 protein is a recombinant viral structural protein that serves as a key antigenic component in prophylactic HPV vaccines, most notably the nonavalent vaccine (Gardasil 9). Produced using recombinant DNA technology in yeast (*Saccharomyces cerevisiae*), the L1 proteins self-assemble into virus-like particles (VLPs) that are morphologically similar to the native HPV capsid but lack the viral genome, rendering them non-infectious. Upon administration, these VLPs trigger a robust humoral immune response, leading to the production of high titers of neutralizing antibodies specific to HPV type 33. These antibodies prevent the virus from binding to and entering host epithelial cells, thereby providing protection against persistent infection and the development of associated pre-cancerous lesions, including cervical intraepithelial neoplasia (CIN), vulvar intraepithelial neoplasia (VIN), and vaginal intraepithelial neoplasia (VaIN). CHU Saint Pierre has been a significant contributor to the clinical development and evaluation of vaccines containing this protein.
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 human papillomavirus type 33 L1 protein.