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Completed Phase 3 Interventional Accepts healthy volunteers Results available

A Study to Evaluate the Immunogenicity of Quadrivalent LAIV (MEDI8662) in Adults 18 to 49 Years of Age

ClinicalTrials.gov ID: NCT00952705

Public ClinicalTrials.gov record NCT00952705. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 3:36 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Partially Blind Active Controlled Study to Evaluate the Immunogenicity of MEDI8662 in Adults 18 to 49 Years of Age

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study was to show that quadrivalent live attenuated influenza vaccine (Q/LAIV-BFS; MEDI8662) was at least as immunogenic as two different forms of the commercial vaccine, FluMist, by comparing the strain-specific antibody levels in the blood.

Study identification

NCT ID
NCT00952705
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
MedImmune LLC
Industry
Enrollment
1,800 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 49 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 2009 (Type not available)
Primary completion
Jan 2010 (Actual)
Completion
Mar 2010 (Actual)
Last update posted
May 3, 2018

2009 – 2010

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
Coastal Clinical Research, Inc. Mobile Alabama 36608 —
Benchmark Research Sacramento California 95816 —
California Research Foundation San Diego California 92103-6204 —
Benchmark Research San Francisco California 94102 —
Tampa Bay Medical Research, Inc. Clearwater Florida 33761 —
Avail Clinical Research, LLC DeLand Florida 32720 —
Miami Research Associates Miami Florida 33143 —
Clinical Research Atlanta Stockbridge Georgia 30281 —
Johnson County Clin-Trials Lenexa Kansas 66219 —
Vince and Associates Clinical Research Overland Park Kansas 66212 —
Benchmark Research Metairie Louisiana 70006 —
Sundance Clinical Research St Louis Missouri 63141 —
Meridian Clinical Research, LLC Omaha Nebraska 68134 —
Regional Clinical Research Endwell New York 13760 —
Rochester Clinical Research Inc. Rochester New York 14609 —
Palmetto Medical Research Mt. Pleasant South Carolina 29464 —
Benchmark Research Austin Austin Texas 78705 —
Benchmark Research Ft. Worth Fort Worth Texas 76135 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00952705, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 3, 2018 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00952705 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →