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Completed Phase 2 Interventional Results available

Formoterol Dose Ranging Study (ACHIEVE Duaklir USA Phase IIb)

ClinicalTrials.gov ID: NCT02796651

Public ClinicalTrials.gov record NCT02796651. 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 Sep 2, 2026, 1:20 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 Randomized, Double-blind, Placebo-controlled, Incomplete Unbalanced, Crossover Study to Assess the Efficacy and Safety of Three Doses of Formoterol Fumarate in Pressair® Compared With Perforomist® Inhalation Solution (20 and 40 μg Open-label) in Moderate to Severe COPD Patients With Reversible Airway Disease.

Brief summary

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

To assess the bronchodilation of three doses of formoterol fumarate (6 μg, 12 μg and 24 μg) twice daily (BID) administered via Pressair® compared to placebo and to open-label nebulized formoterol fumarate (20 μg and 40 μg).

Study identification

NCT ID
NCT02796651
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
132 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 130 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
Jun 29, 2016
Primary completion
Dec 6, 2016
Completion
Dec 6, 2016
Last update posted
Feb 6, 2018

2016

United States locations

U.S. sites
20
U.S. states
9
U.S. cities
20
Facility City State ZIP Site status
Research Site Glendale Arizona 85306
Research Site Phoenix Arizona 85006
Research Site Tempe Arizona 85283
Research Site Celebration Florida 34747
Research Site Clearwater Florida 33756
Research Site DeLand Florida 32720
Research Site Orlando Florida 32825
Research Site Lawrenceville Georgia 30046
Research Site St Louis Missouri 63141
Research Site Las Vegas Nevada 89102
Research Site Charlotte North Carolina 28207
Research Site Gastonia North Carolina 28054
Research Site Medford Oregon 97504
Research Site Portland Oregon 97202
Research Site Easley South Carolina 29640
Research Site Greenville South Carolina 29615
Research Site Rock Hill South Carolina 29372
Research Site Spartanburg South Carolina 29303
Research Site Boerne Texas 78006
Research Site Killeen Texas 76543

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02796651, 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 Feb 6, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02796651 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →