drugset / Trial / NCT06210854
Assessing Administration of pBI-11 Via Electroporation for the Treatment of Patients With HPV16/18+
Phase 2
Recruiting
48 enrolled
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
National Cancer Institute (NCI) · collabPapiVax Biotech, Inc. · collab
RandomizedCrossoverTriple-blindTreatment
Summary
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.
Timeline
- Start
- 2026-06-25
- Primary completion
- 2028-11
- Completion
- 2029-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | pBI-11 | Vaccine | 3 mg | Intramuscular |