Safety, Tolerability, Immunogenicity And CPG Dosage Finding Study of Novartis CpG Adjuvanted Flu Vaccine

PHASE1CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

October 31, 2007

Study Completion Date

May 31, 2008

Conditions
Influenza Infection
Interventions
BIOLOGICAL

Subunit influenza vaccine

0.5 mL single dose vaccine

BIOLOGICAL

Adjuvanted influenza vaccine

0.5 mL single dose vaccine

BIOLOGICAL

Adjuvanted influenza vaccine combined with CpG7909

0.5 ml influenza vaccine combined with 10 mcg of CpG7909

BIOLOGICAL

Adjuvanted influenza vaccine combine with CpG7909

0.5 mL single dose vaccine combined with 30 mcg of CpG7909

BIOLOGICAL

Adjuvanted influenza vaccine combine with CpG7909

0.5 mL single dose vaccine combined with 100 mcg of CpG7909

Trial Locations (1)

6853

Institute for Pharmacokinetic and Analytical Studies, Ligornetto

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Novartis Vaccines

INDUSTRY

lead

Novartis

INDUSTRY

NCT00559975 - Safety, Tolerability, Immunogenicity And CPG Dosage Finding Study of Novartis CpG Adjuvanted Flu Vaccine | Biotech Hunter | Biotech Hunter