A Study to Evaluate the Immunogenicity of Quadrivalent LAIV in Adults 18 to 49 Years of Age

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

1,800

Participants

Timeline

Start Date

March 31, 2009

Primary Completion Date

May 31, 2009

Study Completion Date

October 31, 2009

Conditions
Healthy or Stable Underlying Chronic Medical Condition
Interventions
BIOLOGICAL

Q/LAIV (MEDI3250)

0.2 mL dose at Day 0

BIOLOGICAL

FluMist/B/Yamagata

0.2 mL dose at Day 0

BIOLOGICAL

FluMist/B/Victoria

0.2 mL dose at Day 0

Trial Locations (18)

14609

Rochester Clinical Research, Inc., Rochester

32720

University Clinical Research-Deland, LLC, DeLand

32801

Clinical Research Atlanta, Stockbridge

33024

University Clinical Research, Inc, Pembroke Pines

33126

Pharmax Research Clinic, Inc, Miami

33143

Miami Research Associates, South Miami

37201

Clinical Research Associates, Inc, Nashville

40004

Kentucky Pediatric / Adult Research, Bardstown

63141

Sundance Clinical Research, St Louis

64114

The Center for Pharmaceutical Research, PC, Kansas City

66212

Vince and Associates Clinical Research, Overland Park

68314

Meridian Clinical Research, LLC, Omaha

76135

Benchmark Research, Fort Worth

78705

Benchmark Research, Austin

84088

Advanced Clinical Research, West Jordan

94102

Benchmark Research, San Francisco

95816

Benchmark Research, Sacramento

92103-6204

California Research Foundation, San Diego

Sponsors

Lead Sponsor

All Listed Sponsors
lead

MedImmune LLC

INDUSTRY

NCT00860067 - A Study to Evaluate the Immunogenicity of Quadrivalent LAIV in Adults 18 to 49 Years of Age | Biotech Hunter | Biotech Hunter