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NCT07702656Possibly a fitNot yet recruiting

A trial of SYS6026 vaccine for HPV16/18-related high-grade cervical lesions

High-grade Cervical Intraepithelial Lesions

Part of Women’s health & pregnancy clinical trials.

This trial tests a new vaccine (SYS6026) for women with high-grade cervical lesions caused by HPV type 16 or 18. It aims to see if the vaccine can help the body clear these precancerous cells, potentially avoiding surgery.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
175 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must be 18 or older.
  • You must have a cervical infection with HPV type 16 and/or 18.
  • You must have a high-grade cervical lesion (CIN 2 or CIN 3) confirmed by biopsy.
  • You must be willing to have a biopsy during screening and again at 36 weeks.
  • You must have normal organ function (kidney, liver, blood counts, etc.).
  • If you could become pregnant, you must use reliable birth control for at least a year after the last dose.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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