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Completed Phase 1 Interventional

A Phase I Study in Asthma Patients Evaluating the Effect of Doses of FlutiForm™ on the Amount, if Any, of Cortisol Produced by the Adrenal Glands

ClinicalTrials.gov ID: NCT00657774

Public ClinicalTrials.gov record NCT00657774. 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 23, 2026, 2:09 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 Randomized, Double-Blind, Placebo- and Active-Controlled, Parallel Group, 6-Week Study to Evaluate the Effect of Multiple Doses of FlutiForm™ 250/10 Microgram HFA pMDI Twice Daily, FlutiForm™ 100/10 Microgram HFA pMDI Twice Daily, Prednisone and Placebo on the Hypothalmic-Pituitary-Adrenal Axis in Adult Subjects With Mild to Moderate Asthma.

Study identification

NCT ID
NCT00657774
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
SkyePharma AG
Industry
Enrollment
160 participants

Conditions and interventions

Conditions

Interventions

  • FlutiForm 250/10 ug Drug
  • FlutiForm 100/10 ug Drug
  • Oral Prednisone 10mg Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 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
Mar 31, 2008
Primary completion
Aug 31, 2008
Completion
Aug 31, 2008
Last update posted
Nov 30, 2008

2008

United States locations

U.S. sites
19
U.S. states
11
U.S. cities
19
Facility City State ZIP Site status
Investigational site Phoenix Arizona 85006
Investigational site Anaheim California 92801
Investigational site Long Beach California 90806
Investigational site San Diego California 92120
Investigational site Centennial Colorado 80112
Investigational site Colorado Springs Colorado 80907
Investigational site Denver Colorado 80206
Investigational site Lakewood Colorado 80401
Investigational site DeLand Florida 32720
Investigational Site Pasadena Maryland 21122
Investigational site North Dartmouth Massachusetts 02747
Investigational site Omaha Nebraska 68154
Investigational site Skillman New Jersey 08558
Investigational Site Lake Oswego Oregon 97035
Investigational site Portland Oregon 97213
Investigational site Spartanburg South Carolina 29303
Investigational site El Paso Texas 79902
Investigational site New Braunfels Texas 78130
Investigational site San Antonio Texas 78229

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 NCT00657774, 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 Nov 30, 2008 · Synced Jul 23, 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 NCT00657774 live on ClinicalTrials.gov.

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