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Study identifier: NCT06210854 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Assessing Administration of pBI-11 Via Electroporation for the Treatment of Patients With HPV16/18+

Condition: HPV Infection  ·  Sponsor: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

PhasePhase 2
Planned participants48
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This research is being done to test the safety and feasibility of an investigational DNA vaccine called pBI-11 and to find out what effects, if any, it has on women with persistent human papillomavirus 16 (HPV16+) and/or human papillomavirus (HPV18+) cervical infection. The DNA vaccine is designed to promote an immune response to treat disease caused by HPV types 16 and 18, viruses that can cause cervical cancer. The pBI-11 DNA vaccine or a placebo will be administered intramuscularly using the TriGridTM Delivery System.

This description comes directly from the study's public registry record.

Talk to the study team

Kimberly Levinson, MD  ·  410-955-8240  ·  klevins1@jhmi.edu

Always discuss trial participation with your own doctor first.

Locations (2)

University of Alabama at BirminghamBirmingham, Alabama, United StatesNot Yet Recruiting
Johns Hopkins UniversityBaltimore, Maryland, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06210854