Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Quadrivalent human papillomavirus (types 6, 11, 16, 18) recombinant vaccine (Hansenula polymorpha) is a prophylactic vaccine candidate developed by Shanghai Bowei Biotechnology. It is produced using a recombinant *Hansenula polymorpha* (a methylotrophic yeast) expression system, which is used to generate the L1 major capsid proteins of HPV types 6, 11, 16, and 18. These proteins self-assemble into virus-like particles (VLPs) that are structurally similar to the native virus but lack infectious genetic material. The vaccine is designed to elicit a protective immune response by inducing neutralizing antibodies against the targeted HPV types: types 16 and 18 are high-risk genotypes associated with approximately 70% of cervical cancers, while types 6 and 11 are low-risk genotypes responsible for the majority of genital warts. The vaccine is currently in Phase 3 clinical trials in China, targeting various female age groups (9-26 and 18-45 years) for the prevention of HPV infection, cervical intraepithelial neoplasia (CIN), and related malignancies.
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 quadrivalent human papillomavirus (types 6, 11, 16, 18) recombinant vaccine (hansenula polymorpha).