Femme Homme
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Extrait
Interim analysis: - To assess the efficacy, in the IA population, of RO5217790 compared to placebo in achieving histologic resolution at Month 6 (determined by evaluation of tissue derived from surgical excision of the entire lesion area). Full analysis: - To assess the efficacy of RO5217790 compared to placebo in achieving histologic resolution at Month 6 (determined by evaluation of tissue derived from surgical excision of the entire lesion area) in patients with CIN2/3 associated with HPV16 single infection i.e. stratum 1 (see Section 3.1 of protocol)
Critère d'inclusion
- High grade cervical intraepithelial neoplasia grade 2 or 3 associated with High Risk HPV infection