ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

A Study to Evaluate the Efficacy and Safety of Reslizumab (3.0 mg/kg) in the Reduction of Clinical Asthma Exacerbations in Patients (12-75 Years of Age) With Eosinophilic Asthma

ClinicalTrials.gov ID: NCT01287039

Public ClinicalTrials.gov record NCT01287039. 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 20, 2026, 10:02 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 12-Month, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Reslizumab (3.0 mg/kg) in the Reduction of Clinical Asthma Exacerbations in Patients (12-75 Years of Age) With Eosinophilic Asthma

Study identification

NCT ID
NCT01287039
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Industry
Enrollment
489 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • Reslizumab Drug

Drug

Eligibility (public fields only)

Age range
12 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
Mar 31, 2011
Primary completion
Nov 30, 2013
Completion
Feb 28, 2014
Last update posted
Nov 8, 2021

2011 – 2014

United States locations

U.S. sites
26
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
Teva Investigational Site 58 Scottsdale Arizona
Teva Investigational Site 61 Los Angeles California
Teva Investigational Site 37 Orange California
Teva Investigational Site 56 San Diego California
Teva Investigational Site 34 Colorado Springs Colorado
Teva Investigational Site 52 DeBary Florida
Teva Investigational Site 55 Miami Florida
Teva Investigational Site 18 Valrico Florida
Teva Investigational Site 49 Lexington Kentucky
Teva Investigational Site 65 Louisville Kentucky
Teva Investigational Site 51 Boston Massachusetts
Teva Investigational Site 74 St Louis Missouri
Teva Investigational Site 35 Missoula Montana
Teva Investigational Site 64 Boys Town Nebraska
Teva Investigational Site 68 Rochester New York
Teva Investigational Site 60 The Bronx New York
Teva Investigational Site 30 Winston-Salem North Carolina
Teva Investigational Site 31 Cincinnati Ohio
Teva Investigational Site 62 Columbus Ohio
Teva Investigational Site 50 Oklahoma City Oklahoma
Teva Investigational Site 66 Altoona Pennsylvania
Teva Investigational Site 32 Nashville Tennessee
Teva Investigational Site 63 Boerne Texas
Teva Investigational Site 72 Houston Texas
Teva Investigational Site 38 Richmond Virginia
Teva Investigational Site 33 Madison Wisconsin

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 102 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01287039, 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 8, 2021 · Synced May 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01287039 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →