drugset / Trial / NCT06273553
A Study in Subjects With Human Papillomavirus 16 or 18 Associated Cervical Intraepithelial Neoplasia Grade 2 or 3
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to to evaluate the safety, tolerability, immunogenicity, and efficacy of RG002 Injection in subjects with HPV16/18 associated Cervical Intraepithelial Neoplasia Grade 2 or 3(CIN2/3).
Timeline
- Start
- 2024-03
- Primary completion
- 2026-10
- Completion
- 2027-12