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Completed Phase 3 Interventional Results available

A Study to Evaluate the Efficacy and Safety of Reslizumab (0.3 or 3.0 mg/kg) as Treatment for Patients (12-75 Years of Age) With Eosinophilic Asthma

ClinicalTrials.gov ID: NCT01270464

Public ClinicalTrials.gov record NCT01270464. 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 Jul 22, 2026, 3:26 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 16-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Reslizumab (0.3 or 3.0 mg/kg) as Treatment for Patients (12-75 Years of Age) With Eosinophilic Asthma

Study identification

NCT ID
NCT01270464
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Industry
Enrollment
315 participants

Conditions and interventions

Interventions

  • Reslizumab Drug
  • Placebo 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
Jan 31, 2011
Primary completion
Aug 31, 2013
Completion
Aug 31, 2013
Last update posted
Jun 5, 2016

2011 – 2013

United States locations

U.S. sites
26
U.S. states
12
U.S. cities
24
Facility City State ZIP Site status
Teva Investigational Site 12 Anaheim California
Teva Investigational Site 11 Fountain Valley California
Teva Investigational Site 43 Los Angeles California
Teva Investigational Site 4 Orange California
Teva Investigational Site 15 Walnut Creek California
Teva Investigational Site 2 Colorado Springs Colorado
Teva Investigational Site 24 Largo Florida
Teva Investigational Site 27 Miami Florida
Teva Investigational Site 5 Miami Florida
Teva Investigational Site 19 Tallahassee Florida
Teva Investigational Site 17 Trinity Florida
Teva Investigational Site 18 Valrico Florida
Teva Investigational Site 6 Lilburn Georgia
Teva Investigational Site 3 Savannah Georgia
Teva Investigational Site 7 Iowa City Iowa
Teva Investigational Site 8 Omaha Nebraska
Teva Investigational Site 26 Summit New Jersey
Teva Investigational Site 20 Cincinnati Ohio
Teva Investigational Site 1 Medford Oregon
Teva Investigational Site 73 Lincoln Rhode Island
Teva Investigational Site 9 Providence Rhode Island
Teva Investigational Site 21 Charleston South Carolina
Teva Investigational Site 16 Fort Worth Texas
Teva Investigational Site 10 Houston Texas
Teva Investigational Site 14 San Antonio Texas
Teva Investigational Site 45 San Antonio Texas

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 63 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01270464, 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 Jun 5, 2016 · Synced Jul 22, 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 NCT01270464 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →