Clin2
NCT07668960Possibly a fitNot yet recruiting

Testing a new shot for HPV-related cervical pre-cancer

High-grade Squamous Intraepithelial Lesions of the Cervix Associated With Human Papillomavirus (HPV) Type 16 and/or HPV Type 18 Infection

Part of Infections clinical trials.

This trial tests an experimental shot, BBM-C101, for women with a specific type of cervical pre-cancer caused by HPV types 16 or 18. The goal is to see if the shot is safe and can help the body fight the infection, possibly eliminating the abnormal cells.

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

Phase
Phase 1/Phase 2
Enrollment
60 people
Ages
18 years to 55 years
Study type
Interventional

Who can take part

  • You must have a cervical biopsy showing high-grade pre-cancer (HSIL) linked to HPV type 16 or 18.
  • Your colposcopy (a special magnified exam of the cervix) must be clear enough to see the area, and a sample from inside the cervical canal must not show cancer
  • You cannot be pregnant or nursing, and if you could become pregnant, you must use effective birth control for a year after the shot
  • You must not have had previous treatment for HPV or this cervical condition, or any prior HPV vaccine except the standard preventive ones.
  • You cannot have certain other infections, autoimmune diseases, or unstable heart or blood vessel problems.

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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