Technology evaluation: T-cell activator, Xenova

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

TA-HPV (therapeutic antigen-human papilloma virus) is a vaccine being developed by Xenova (formerly Cantab) for the potential treatment of cervical cancer. The antigen is intended to activate HPV-specific cytotoxic T-cells to attack tumor cells containing the viral antigen. Over 70% of patients with cervical cancer have tumor cells containing papillomavirus DNA [173070]. TA-HPV has reached phase IIa trials in 60 patients with high-grade anogenital intraepithelial neoplasia, including VIN3 (grade 3 vulvar intraepithelial neoplasia), to evaluate clinical efficacy [381386], [427159], [429895]. In addition, a phase II 'prime-boost' study of TA-HPV in combination with TA-CIN has been initiated at three centers across the UK [427159]. In November 2000, Lehman Brothers predicted that the product would be launched in 2005, peak sales of £100 million in 2010, with a 25% probability of reaching the market [391876].

Original languageEnglish (US)
Pages (from-to)585-588
Number of pages4
JournalCurrent Opinion in Molecular Therapeutics
Volume3
Issue number6
StatePublished - Dec 1 2001

ASJC Scopus subject areas

  • Molecular Medicine
  • Molecular Biology
  • Genetics
  • Pharmacology
  • Drug Discovery
  • Genetics(clinical)

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