Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Gardasil is a quadrivalent recombinant vaccine developed by Merck & Co. (MSD) to prevent infections and associated diseases caused by Human Papillomavirus (HPV) types 6, 11, 16, and 18. The vaccine is composed of purified virus-like particles (VLPs) of the major capsid (L1) protein of each of the four HPV types, which are produced via recombinant DNA technology in *Saccharomyces cerevisiae*. HPV types 16 and 18 are high-risk genotypes responsible for approximately 70% of cervical cancers and a significant proportion of other HPV-related malignancies, including vulvar, vaginal, and anal cancers. HPV types 6 and 11 are low-risk genotypes responsible for approximately 90% of genital warts (condyloma acuminata). The vaccine works by inducing a humoral immune response, specifically the production of neutralizing antibodies, which prevents the virus from entering host cells and establishing infection. It is indicated for use in both females and males, typically starting at age 9, to prevent cervical, vulvar, vaginal, and anal cancers, as well as genital warts and precancerous or dysplastic lesions.
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 quadrivalent (types 6, 11, 16, 18) vaccine, recombinant (Merck & Co.).