Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2008-004604-31Phase 2Completed
Phase 2, randomised trial in cervical intraepithelial neoplasia (CIN) and cervical intraepithelial neoplasia grade 1 comparing HAL PDT (Cevira) with Placebo PDT (2 arms). Primary endpoint: Complete response rate at 6 months. Started Aug 2008; status: completed.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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