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NWRD09 for Persistent Cervical HPV16 Infection

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Study First Submitted
This is a randomized, double-blind, placebo controlled study to determine the efficacy and safety of NWRD09 in adult women with persistent cervical HPV16 infection.
Trial Details
NCT Number NCT07710703
Lead Sponsor Newish Biotech (Wuxi) Co., Ltd.
Conditions
(from sponsor)		 Persistent Cervical HPV16 Infection
Related terms Persistent Infection
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov