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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 Oct 21, 2026, 7:48 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

Brief summary

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

This is a Phase 3, multicenter, randomized, double-blind, placebo-controlled, parallel-group study to evaluate the efficacy, safety, and immunogenicity of treatment with reslizumab in patients with eosinophilic asthma.

Study identification

NCT ID
NCT01287039
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
489 participants

Conditions and interventions

Interventions

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
Apr 2011 (Type not available)
Primary completion
Dec 2013 (Actual)
Completion
Mar 2014 (Actual)
Last update posted
Nov 9, 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 9, 2021 · Synced Oct 21, 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 public registry record, listed eligibility criteria, and available contact information for NCT01287039 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →