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Terminated Phase 2 Interventional Accepts healthy volunteers Results available

A Study to Evaluate the Efficacy of MEDI7510 in Older Adults

ClinicalTrials.gov ID: NCT02508194

Public ClinicalTrials.gov record NCT02508194. 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 May 6, 2026, 8:53 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 Phase 2b Randomized, Double-blind Study to Evaluate the Efficacy of MEDI7510 for the Prevention of Acute Respiratory Syncytial Virus-associated Respiratory Illness in Older Adults

Study identification

NCT ID
NCT02508194
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
MedImmune LLC
Industry
Enrollment
1,900 participants

Conditions and interventions

Interventions

  • IIV Biological
  • MEDI7510 Biological
  • Placebo Other

Biological · Other

Eligibility (public fields only)

Age range
60 Years to 99 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
Sep 28, 2015
Primary completion
Sep 8, 2016
Completion
Nov 6, 2016
Last update posted
Dec 25, 2017

2015 – 2016

United States locations

U.S. sites
30
U.S. states
16
U.S. cities
30
Facility City State ZIP Site status
Research Site Sacramento California 95864
Research Site San Francisco California 94108
Research Site Aurora Colorado 80045
Research Site Littleton Colorado 80127
Research Site Lady Lake Florida 32159
Research Site Miami Florida 33143
Research Site Orlando Florida 32806
Research Site Savannah Georgia 31406
Research Site Champaign Illinois 61820
Research Site Chicago Illinois 60654
Research Site Council Bluffs Iowa 51503
Research Site Augusta Kansas 67010
Research Site Wichita Kansas 67205
Research Site Edina Minnesota 55435
Research Site Cincinnati Missouri 45249
Research Site Kansas City Missouri 64114
Research Site Bellevue Nebraska 68005
Research Site Norfolk Nebraska 68701
Research Site Omaha Nebraska 68134
Research Site Rochester New York 14621
Research Site Charlotte North Carolina 28209
Research Site Hickory North Carolina 28602
Research Site Raleigh North Carolina 27609
Research Site Rocky Mount North Carolina 27804
Research Site Winston-Salem North Carolina 27103
Research Site Akron Ohio 44311
Research Site Dakota Dunes South Dakota 57049
Research Site Knoxville Tennessee 37912
Research Site Nashville Tennessee 37212
Research Site Murray Utah 84123

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 31 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02508194, 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 Dec 25, 2017 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02508194 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →