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Completed Phase 2 Interventional Results available

A Study in Asthmatic Children (6 to <12 Yrs) Comparing Single Doses of Formoterol and Foradil® Evaluating Efficacy

ClinicalTrials.gov ID: NCT01136655

Public ClinicalTrials.gov record NCT01136655. 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 19, 2026, 10:04 PM 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 Phase 2, Randomized, Blinded, 5-period Cross-over, Placebo and Active Controlled, Multicenter, Dose-finding Study Comparing Single Doses of Formoterol 2.25 µg, 4.5 µg, and 9 µg Delivered Via Symbicort pMDI and Foradil® 12 µg Evaluating the Relative Bronchodilating Effects and Safety in Children

Brief summary

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

This purpose of the study is to investigate the bronchodilating effects of 3 different dosages of formoterol given in combination with budesonide as Symbicort pMDI.

Study identification

NCT ID
NCT01136655
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
54 participants

Conditions and interventions

Eligibility (public fields only)

Age range
6 Years to 11 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
Sep 2010 (Type not available)
Primary completion
Dec 2011 (Actual)
Completion
Dec 2011 (Actual)
Last update posted
Oct 31, 2013

2010 – 2011

United States locations

U.S. sites
20
U.S. states
9
U.S. cities
20
Facility City State ZIP Site status
Research Site Huntington California — —
Research Site Long Beach California — —
Research Site Mission Viejo California — —
Research Site Orange California — —
Research Site Rolling Hills Estate California — —
Research Site Sarasota Florida — —
Research Site Omaha Nebraska — —
Research Site Morrisville North Carolina — —
Research Site Raleigh North Carolina — —
Research Site Eugene Oregon — —
Research Site Lake Oswego Oregon — —
Research Site Medford Oregon — —
Research Site Portland Oregon — —
Research Site Altoona Pennsylvania — —
Research Site Upland Pennsylvania — —
Research Site Charleston South Carolina — —
Research Site El Paso Texas — —
Research Site San Antonio Texas — —
Research Site Waco Texas — —
Research Site Springfield Virginia — —

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 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01136655, 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 Oct 31, 2013 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01136655 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →