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COMPLETED Phase 3

Study of Levalbuterol, Racemic Albuterol and Placebo in Subjects Twelve Years of Age and Older With Asthma

NCT00073840 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to investigate the efficacy of levalbuterol 90 ug (2 actuations, 45 ug each) versus placebo (2 actuations) in the treatment and prevention of bronchoconstriction in adolescent and adult subjects with asthma, with all treatments administered 4 times a day (QID).

Conditions Studied

Interventions

  • DRUG levalbuterol

Study Locations (20)

California

  • Integrated Research Group — Corona
  • Radiant Research, Inc. — Encinitas
  • Allergy & Asthma Specialists Medical Group — Huntington Beach
  • Asthma, Allergy & Respiratory Care Center — Long Beach
  • Allergy Research Foundation, Inc. — Los Angeles
  • Madera Family Medical Group — Madera
  • Southern California Research — Mission Viejo
  • Comprehensive Allergy Services — Oakland
  • Clinical Trials of Orange County — Orange
  • Allergy Associates Medical Group — San Diego
  • Allergy & Asthma Medical Group & Research Center — San Diego
  • Allergy & Asthma Assoc. of Santa Clara Valley Research Center — San Jose
  • West Coast Clinical Trials — Signal Hill
  • Allergy & Asthma Medical Group of Diablo Valley, Inc. — Walnut Creek

Georgia

  • Watts Medical Research — Barnesville
  • The Allergy & Asthma Clinical Research Center — Conyers
  • Aeroallergy Research Laboratories of Savannah, Inc. — Savannah

Alabama

  • Allergy & Asthma Center, LLC — Oxford

Arizona

  • Alta Clinical Research — Tucson

Colorado

  • 1st Allergy & Asthma Clinical Research Ctr — Thornton

Trial Details

FieldValue
Enrollment Target 386 participants
Start Date 2002-12
Est. Completion 2003-06
Phase Phase 3

Sponsor

Sumitomo Pharma America

65 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00073840

The ClinicalTrials.gov registry entry for NCT00073840 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 386 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sumitomo Pharma America, which has 65 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 1 intervention — of which levalbuterol 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: NCT00073840 reports 20 study locations spanning 5 distinct geographic areas — top geographies include California, Georgia, 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 NCT00073840 about?

NCT00073840 is a clinical study titled "Study of Levalbuterol, Racemic Albuterol and Placebo in Subjects Twelve Years of Age and Older With Asthma". The primary objective of this study is to investigate the efficacy of levalbuterol 90 ug (2 actuations, 45 ug each) versus placebo (2 actuations) in the treatment and prevention of bronchoconstriction in adolescent and adult subjects with asthma, with all treatments administered 4 times a day (QID).

What is the current status of trial NCT00073840?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 386 participants. The study started on 2002-12. Estimated completion is 2003-06.

What conditions does trial NCT00073840 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 NCT00073840?

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

Who is sponsoring clinical trial NCT00073840?

This trial is sponsored by Sumitomo Pharma America, which has 65 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00073840 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Colorado, Georgia. 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