"Immunogenicity and Safety of Verorab® in a One-week Intradermal Post-exposure Prophylaxis Regimen"

PHASE3CompletedINTERVENTIONAL
Enrollment

600

Participants

Timeline

Start Date

June 29, 2012

Primary Completion Date

November 14, 2018

Study Completion Date

November 14, 2018

Conditions
Rabies
Interventions
BIOLOGICAL

PVRV

0.1 mL, 4 site 'one week' (4-4-4-0-0) administered intradermally

BIOLOGICAL

PVRV and pERIG Favirab®

0.1 mL of vaccine administered intradermally in 4 site 'one week' (4-4-4-0-0) regimen, and pERIG Favirab® (volume to be calculated according to the patient' body weight) infiltrated into and around wound(s)

BIOLOGICAL

PVRV and pERIG Favirab®

0.1 mL of vaccine administered intradermally in 2-site TRC (2-2-2-0-2) regimen, and pERIG Favirab® (volume to be calculated according to the patient' body weight) infiltrated into and around wound(s)

Trial Locations (1)

1781

City of Muntinlupa

All Listed Sponsors
lead

Sanofi Pasteur, a Sanofi Company

INDUSTRY

NCT01622062 - "Immunogenicity and Safety of Verorab® in a One-week Intradermal Post-exposure Prophylaxis Regimen" | Biotech Hunter | Biotech Hunter