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Completed Phase 2 Interventional Results available

Study to Evaluate the Efficacy and Safety of MEDI-563 in Adults With Uncontrolled Asthma

ClinicalTrials.gov ID: NCT01238861

Public ClinicalTrials.gov record NCT01238861. 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 Sep 5, 2026, 1:36 PM 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, Dose-ranging Study to Evaluate the Efficacy and Safety of MEDI-563 in Adults With Uncontrolled Asthma

Brief summary

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

The primary objective of the study is to evaluate the effect of multiple-dose subcutaneous administrations of MEDI-563 on adults with uncontrolled asthma.

Study identification

NCT ID
NCT01238861
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
MedImmune LLC
Industry
Enrollment
964 participants

Conditions and interventions

Conditions

Interventions

Biological · Other

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Nov 30, 2010
Primary completion
Feb 28, 2013
Completion
Jul 31, 2013
Last update posted
Nov 16, 2016

2010 – 2013

United States locations

U.S. sites
27
U.S. states
20
U.S. cities
27
Facility City State ZIP Site status
Research Site Birmingham Alabama
Research Site Los Angeles California
Research Site Orange California
Research Site San Diego California
Research Site Stockton California
Research Site Colorado Springs Colorado
Research Site Denver Colorado
Research Site Waterbury Connecticut
Research Site Kissimmee Florida
Research Site Tampa Florida
Research Site Stockbridge Georgia
Research Site Normal Illinois
Research Site Baltimore Maryland
Research Site Rochester Minnesota
Research Site St Louis Missouri
Research Site Bellevue Nebraska
Research Site Summit New Jersey
Research Site Rochester New York
Research Site Winston-Salem North Carolina
Research Site Cincinnati Ohio
Research Site Oklahoma City Oklahoma
Research Site Blue Bell Pennsylvania
Research Site Pittsburgh Pennsylvania
Research Site Warwick Rhode Island
Research Site Boerne Texas
Research Site San Antonio Texas
Research Site Seattle Washington

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 47 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01238861, 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 Nov 16, 2016 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01238861 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →