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RECRUITINGPHASE2

Evaluation of NWRD08 for HPV-16 and/or HPV-18 Related Cervical HSIL

NCT07175662

This is a randomized, double-blind, placebo controlled Phase 2 study to determine the efficacy and safety of NWRD08 administered by intramuscular (IM) injection followed by electroporation (EP) in adult women with histologically confirmed cervical high grade squamous intraepithelial lesion (HSIL) (cervical intraepithelial neoplasia grade 2 \[CIN2\] or grade 3 \[CIN3\]) associated with human papillomavirus (HPV) 16 and/or HPV18.

High-grade Squamous Intraepithelial Lesion (HSIL)

Newish Biotech (Wuxi) Co., Ltd.150 participantsStarted Nov 2025

Beijing, Beijing Municipality, China • Beijing, Beijing Municipality, China • Beijing, Beijing Municipality, China +2 more locations

Data from ClinicalTrials.govTerms