An Exploratory Safety and Immunogenicity Study of HPV16+ Immunotherapy VB10.16 in Women With HSIL; CIN 2/3)

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

August 31, 2015

Primary Completion Date

January 31, 2019

Study Completion Date

January 31, 2019

Conditions
High Grade Cervical Intraepithelial Neoplasia
Interventions
BIOLOGICAL

VB10.16 Immunotherapy (DNA vaccine)

Patients will receive 3 vaccinations of 3 mg VB10.16 at the pre-specified time points. VB10.16 will be administered intramuscularly in the area over the lateral deltoid muscle.

Trial Locations (4)

20246

Universitätsklinikum Hamburg-Eppendorf, Hamburg

30159

IZD Institut für Zytologie und Dysplasie, Hanover

30625

Medical School Hanover, Hanover

38440

Klinikum Wolfsburg, Wolfsburg

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Theradex

INDUSTRY

collaborator

Vaccibody AS

INDUSTRY

lead

Nykode Therapeutics ASA

INDUSTRY