HUMAN PAPILLOMA VIRUS Clinical Trial
Official title:
A Double-blind, Randomised, Placebo-controlled, Phase II Study to Evaluate ProCervix Efficacy to Clear HPV 16 and HPV 18 Infection in Women With Normal Cytology or ASCUS/LSIL
Human Papillomavirus (HPV) 16 and HPV 18 (the two virus genotypes targeted by the ProCervix
vaccine) are the most common HPV genotypes associated with at least 70% of squamous cell
carcinomas and 82% of adenocarcinomas of the cervix The strategy of therapeutic vaccination
with ProCervix is to activate and enhance the patient's cellular immune response to HPV .
The therapeutic vaccine will be used for women infected by HPV 16, HPV 18, or both. The
vaccine targets these HPV infected women with normal or mild cervical cellular dyskaryosis
as detectable infections with oncogenic potential.
This will be a double-blind, randomised, placebo-controlled, parallel group study assessing
the efficacy of ProCervix or placebo (concomitantly administered with imiquimod cream).
ProCervix will be delivered with a topical agent, imiquimod, applied to the injection sites
as a vaccine adjuvant.
The population proposed for this study represents an otherwise healthy female population who
are infected with HPV 16 and/or HPV 18. The safety and tolerability of this therapeutic
vaccine has been shown in the ongoing Phase I study, and the proposed population may in
theory derive benefit from this vaccine.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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