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NCT07702656Possibly a fitNot yet recruiting

Study of SYS6026 injection for high-grade cervical lesions linked to HPV 16 or 18

High-grade Cervical Intraepithelial Lesions

Part of Cancer, Infections, Women’s health & pregnancy clinical trials.

This study tests an investigational injection called SYS6026 for people with high-grade cervical precancerous lesions (CIN 2 or 3) caused by HPV types 16 or 18. The goal is to see if the injection can help the body clear the HPV and reduce or eliminate the abnormal cells, possibly 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 years or older.
  • You must have a cervical infection with HPV type 16 and/or 18, confirmed by a test.
  • You must have a biopsy showing high-grade cervical lesions (CIN 2 or CIN 3) within the last 3 months.
  • The doctor must be able to see the entire area where the cervix meets the cervical canal and the lesions must be large enough to be observed during the study.
  • You must agree to have a biopsy before starting and a follow-up biopsy or surgery at 36 weeks after the first injection.
  • You must be in generally good health, with normal blood counts, liver, kidney, and heart function, and no uncontrolled high blood pressure or fever.
  • If you can become pregnant, you must use reliable birth control during the study and for at least one year after the last dose, and have a negative pregnancy test before starting.

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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