Immunogenicity and Safety of Three Formulations of Dengue Vaccines in Healthy Adults Aged 18 to 45 Years in the US

PHASE2CompletedINTERVENTIONAL
Enrollment

260

Participants

Timeline

Start Date

April 17, 2008

Primary Completion Date

December 31, 2009

Study Completion Date

February 28, 2010

Conditions
Dengue FeverDengue Hemorrhagic FeverDengue Virus
Interventions
BIOLOGICAL

Tetravalent CYD Dengue Vaccine , 5555 formulation

A 0.5 mL dose, Subcutaneous at 0, 6, and 12 months, respectively.

BIOLOGICAL

Tetravalent CYD Dengue Vaccine , 5553 formulation

A 0.5 mL dose, Subcutaneous at 0, 6, and 12 months, respectively

BIOLOGICAL

Tetravalent CYD Dengue Vaccine, 4444 formulation

A 0.5 mL dose, Subcutaneous at 0, 6, and 12 months, respectively

Trial Locations (5)

35126

Investigational Site 004, Hoover

65802

Investigational Site 003, Springfield

70119

Investigational Site 001, New Orleans

92103

Investigational Site 002, San Diego

94589

Investigational Site 005, Vallejo

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Sanofi

INDUSTRY

NCT00617344 - Immunogenicity and Safety of Three Formulations of Dengue Vaccines in Healthy Adults Aged 18 to 45 Years in the US | Biotech Hunter | Biotech Hunter