This study will test the efficacy and safety of different routes of administration of a
DNA vaccine in patients with HPV16+ CIN2/3. Subjects will be enrolled in one of six
treatment groups. Subjects enrolled in the first two groups will receive vaccination
intradermally with a needle-free delivery device. Subjects enrolled in groups 3 and 4
will receive vaccination intramuscularly. Subjects enrolled in groups 5 and 6 will
receive vaccine intralesionally.
Additional locations may be listed on ClinicalTrials.gov for NCT00988559.
Locations matching your search criteria
United States
Maryland
Baltimore
Johns Hopkins University/Sidney Kimmel Cancer CenterStatus: Active
Contact: Cornelia Liu Trimble
Phone: 410-955-8804
Primary Objectives
- To evaluate the feasibility and toxicity of vaccination in women with CIN2/3 caused
by HPV16
- To evaluate the effect of vaccination on histology
- To compare immunogenicity of three different routes of administration: intradermal
(ID), intramuscular (IM), intralesional (IL).
Secondary Objectives:
- To evaluate changes in HPV viral load
- To evaluate the cellular immune response to vaccination
- To evaluate the humoral immune response to vaccination
- To evaluate local tissue immune response
- To correlate measures of immune response with clinical response
- To correlate measures of immune response with those observed in the preclinical
model
Lead OrganizationJohns Hopkins University/Sidney Kimmel Cancer Center