A Phase 3 Clinical Trial to Evaluate Long-term Immunogenicity and Boostability of Purified Chick-Embryo Cell Rabies Vaccine in Adults Following Primary Series of Pre/Exposure Prophylaxis.

PHASE3CompletedINTERVENTIONAL
Enrollment

459

Participants

Timeline

Start Date

October 5, 2015

Primary Completion Date

December 23, 2022

Study Completion Date

December 23, 2022

Conditions
Virus DiseasesRabies
Interventions
BIOLOGICAL

Rabipur

Participants in all the groups received Rabipur vaccine booster dose, administered intramuscularly in the deltoid region of the non-dominant arm.

PROCEDURE

Blood sampling

Blood samples were drawn from all participants at Day 1 and then at subsequent year intervals from extension study Day 1 onwards.

BIOLOGICAL

Purified Chick-Embryo Cell Rabies Vaccine

1 booster dose of 1.0 mL of Purified Chick-Embryo Cell Rabies Vaccine intramuscular (IM).

Trial Locations (7)

1090

GSK Investigational Site, Vienna

8001

GSK Investigational Site, Zurich

10117

GSK Investigational Site, Berlin

13353

GSK Investigational Site, Berlin

18057

GSK Investigational Site, Rostock

20359

GSK Investigational Site, Hamburg

80802

GSK Investigational Site, Munich

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY

NCT02545517 - A Phase 3 Clinical Trial to Evaluate Long-term Immunogenicity and Boostability of Purified Chick-Embryo Cell Rabies Vaccine in Adults Following Primary Series of Pre/Exposure Prophylaxis. | Biotech Hunter | Biotech Hunter