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Professor Xia Ningshao's team published the final analysis results of the first domestic bivalent human papillomavirus vaccine Phase III clinical trial in The Lancet Infectious Diseases

 Last Update: 2022-09-09
 Source: Internet
 Author: User

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^{The research team carried out a multi-center, randomized, double-blind, controlled (hepatitis E vaccine Yikening ?} ) Phase III clinical trial of Xinkening ^? based on 5 sites across the country.

^The results of the final analysis of the 66-month follow-up of the Phase III clinical trial of Cincogene® showed that in the per-protocol set (PPS) population, the vaccine was effective against HPV type 16 and/or 18 infection-related lesion endpoints (CIN2+ and/or or VIN2+ and/or VaIN2+) protection was 100.

Recently, the research results are titled "Efficacy, Safety, and Immunogenicity of an Escherichia coli-Produced Human Papillomavirus (types 16 and 18) L1 Virus-like-particle Vaccine: end-of-study analysis of a phase 3 double-blind, The randomized controlled trial" paper is published online in The Lancet Infectious Diseases

Paper link:National Research Center for Infectious Disease Diagnostic Reagents and Vaccine Engineering Technology)

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