drugset / Trial / NCT06276101

NWRD08 DNA Plasmid for HPV-16 and/or HPV-18 Related Cervical HSIL

NCT06276101 ↗

Phase 1 Completed 9 enrolled Newish Technology (Beijing) Co., Ltd.
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a single-arm, open label, multi-center Phase 1 clinical study to evaluate the safety and tolerability of HPV-16 and HPV-18-targeted DNA plasmid vaccine (NWRD08) in patients HPV-16 and/or HPV-18 related cervical HSIL.

Timeline

Start
2024-05-07
Primary completion
2025-02-19
Completion
2025-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject NWRD08 Vaccine 1 mg Intramuscular
Subject NWRD08 Vaccine 4 mg Intramuscular
Subject NWRD08 Vaccine 8 mg Intramuscular