Clinical Trial

Evaluation of NWRD09 for Female Participants With Persistent HPV16 Infection

Not Yet Recruiting Phase 1/2
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Summary
This is a two-part, phase I/IIa study, intended to evaluate the safety, tolerability, immunogenicity, and efficacy of NWRD09 in female participants with persistent HPV16 infection, and to determine the MTD, and/or RP2D of NWRD09.
Trial Details
NCT Number NCT07536282
Lead Sponsor Newish Biotech (Wuxi) Co., Ltd.
Conditions Persistent HPV16 Infection
Enrollment 78 participants
Start Date 2026-10
Primary Completion 2027-09 (estimated)
Study Completion 2027-11 (estimated)
Updated on ClinicalTrials.gov 2026-04-17