Immunogenicity and Safety of MenACWY in Infants (6 & 12 Months)

PHASE2CompletedINTERVENTIONAL
Enrollment

175

Participants

Timeline

Start Date

June 30, 2005

Primary Completion Date

November 30, 2006

Study Completion Date

November 30, 2006

Conditions
Meningococcal Meningitis
Interventions
BIOLOGICAL

MenACWY-CRM

Subjects received the full dose (0.5 mL) of MenACWY-CRM, obtained by extemporaneous mixing of lyophilized MenA powder component and the MenCWY suspension, administered by IM injection into the anterolateral area of the right thigh.

BIOLOGICAL

MenC-CRM

One dose (0.5 mL) of MenC-CRM was obtained by extemporaneous mixing just before injection of the lyophilized MenC component and a saline solvent, administered by IM injection into the arm region.

BIOLOGICAL

DTaP-Hib-IPV

BIOLOGICAL

PC7

One dose (0.5 mL) of PC7, supplied in pre-filled syringe, administered by IM injection into the anterolateral area of the left thigh.

BIOLOGICAL

MMR

BIOLOGICAL

Varicella

Trial Locations (3)

K1H 8L1

Children's Hospital of Eastern Ontario Research Institute, Ottawa

K1S 0G8

Herridge Community Health Clinic, Ottawa

B3K 6R8

Clinical Trials Research Center, Department of Pediatrics, Dalhousie University, IWK Health Center, Halifax

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novartis Vaccines

INDUSTRY

NCT00310856 - Immunogenicity and Safety of MenACWY in Infants (6 & 12 Months) | Biotech Hunter | Biotech Hunter