Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED Phase 3

Study of Reslizumab in Participants With Uncontrolled Asthma and Elevated Blood Eosinophils

NCT02452190 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to determine the effect of reslizumab (110 mg) administered subcutaneously every 4 weeks on clinical asthma exacerbations in adults and adolescents with asthma and elevated blood eosinophils who are inadequately controlled on standard-of-care asthma therapy.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Reslizumab

Study Locations (20)

California

  • Teva Investigational Site 13215 — Bakersfield
  • Teva Investigational Site 13181 — Canoga Park
  • Teva Investigational Site 13254 — Fresno
  • Teva Investigational Site 13216 — Huntington Beach
  • Teva Investigational Site 13247 — Long Beach
  • Teva Investigational Site 13205 — Napa
  • Teva Investigational Site 13764 — San Jose
  • Teva Investigational Site 13252 — Stockton
  • Teva Investigational Site 13251 — Walnut Creek

Florida

  • Teva Investigational Site 13196 — Aventura
  • Teva Investigational Site 13256 — Fort Lauderdale
  • Teva Investigational Site 13203 — Kissimmee
  • Teva Investigational Site 13197 — Miami
  • Teva Investigational Site 13220 — Miami
  • Teva Investigational Site 13243 — Miami

Alabama

  • Teva Investigational Site 13212 — Birmingham

Arizona

  • Teva Investigational Site 13241 — Flagstaff

Arkansas

  • Teva Investigational Site 13194 — Glendale

Colorado

  • Teva Investigational Site 13229 — Denver

Connecticut

  • Teva Investigational Site 13766 — Waterbury

Trial Details

FieldValue
Enrollment Target 468 participants
Start Date 2015-09-28
Est. Completion 2018-01-31
Phase Phase 3

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02452190

The ClinicalTrials.gov registry entry for NCT02452190 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 468 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Teva Branded Pharmaceutical Products R&D, which has 103 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Asthma appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02452190 reports 20 study locations spanning 7 distinct geographic areas — top geographies include California, Florida, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02452190 about?

NCT02452190 is a clinical study titled "Study of Reslizumab in Participants With Uncontrolled Asthma and Elevated Blood Eosinophils". The primary objective of this study is to determine the effect of reslizumab (110 mg) administered subcutaneously every 4 weeks on clinical asthma exacerbations in adults and adolescents with asthma and elevated blood eosinophils who are inadequately controlled on standard-of-care asthma therapy.

What is the current status of trial NCT02452190?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 468 participants. The study started on 2015-09-28. Estimated completion is 2018-01-31.

What conditions does trial NCT02452190 study?

This clinical trial studies the following conditions: Asthma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02452190?

The interventions under investigation include: Placebo (DRUG), Reslizumab (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02452190?

This trial is sponsored by Teva Branded Pharmaceutical Products R&D, which has 103 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02452190 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial