Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06319963Phase 2Recruiting
Phase 2, open-label trial of Lenti-HPV-07 in cervical carcinoma and human papillomavirus-positive oropharyngeal squamous cell carcinoma (2 arms), sponsored by TheraVectys. Primary endpoints: Safety and Tolerability at 12 months and Optimal Biological Dose at 28 days. Started Aug 2024; status: recruiting.
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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