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Search / Trial NCT00393991

Comparison of New Combination Inhaler (FlutiForm HFA MDI 100/10 µg) Versus Fluticasone and Formoterol Administered Alone, and Placebo, in Patients With Asthma

Launched by SKYEPHARMA AG · Oct 30, 2006

Trial Information

Current as of July 21, 2025

Completed

Keywords

Asthma Fluticasone Propionate Formoterol Fumarate Pressurized Metered Dose Inhaler Hydrofluoroalkane Mild To Moderate Asthma

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Ages eligible for study: 12 years and above; genders eligible for study: both; prior steroid use: steroid-requiring or steroid-free.
  • Inclusion Criteria:
  • History of asthma for at least 12 months.
  • For steroid-requiring patients, documented use of inhaled corticosteroid for at least 4 weeks prior to Screening Visit
  • For steroid-free patients, no history of inhaled steroid asthma medication for at least 12 weeks prior to Screening Visit.
  • Demonstrate FEV-1 of 60-85% of predicted normal values at Screening and Baseline Visit.
  • Documented reversibility of 15% within 12 months of Screening or at Screening Visit (15% increase from pre-FEV-1 levels following albuterol inhalation or nebulized albuterol administration).
  • Symptoms of Asthma during Run-in
  • Females of childbearing potential must have a negative urine pregnancy test at Screening and Baseline Visits. Females are eligible only if they are not pregnant or lactating, and are either sterile, or using acceptable methods of contraception.
  • Must otherwise be healthy.
  • Provide written informed consent. Wishes of minors must be respected.
  • Exclusion Criteria:
  • Life-threatening asthma within past year or during Run-In Period.
  • History of systemic corticosteroid medication within 3 months before Screening Visit.
  • History of omalizumab use within past 6 months.
  • History of leukotriene receptor antagonist use, e.g. montelukast, within past week.
  • Current evidence or history of any clinically significant disease or abnormality including uncontrolled hypertension, uncontrolled coronary artery disease, congestive heart failure, myocardial infarction, or cardiac dysrhythmia.
  • Upper or lower respiratory infection within 4 weeks prior to Screening Visit or during Run-In Period.
  • Significant, non-reversible, pulmonary disease (e.g., chronic obstructive pulmonary disease \[COPD\], cystic fibrosis, bronchiectasis).
  • Known Human Immunodeficiency Virus (HIV)-positive status.
  • Smoking history equivalent to "10 pack years".
  • Current smoking history within 12 months prior to Screening Visit.
  • Current evidence or history of alcohol and/or substance abuse within 12 months prior to Screening Visit.
  • Patients who are confined in institution

About Skyepharma Ag

Skyepharma AG is a leading global pharmaceutical company specializing in the development of innovative drug delivery systems and formulations. With a strong focus on enhancing the bioavailability and therapeutic effectiveness of pharmaceutical compounds, Skyepharma leverages advanced technologies to address unmet medical needs across various therapeutic areas. The company is committed to delivering high-quality products through rigorous clinical trials and regulatory compliance, ensuring that its solutions meet the highest standards of safety and efficacy. With a dedicated team of experts and a robust pipeline, Skyepharma AG is poised to make significant contributions to the advancement of modern medicine.

Locations

Scottsdale, Arizona, United States

Ocala, Florida, United States

Indianapolis, Indiana, United States

Bethesda, Maryland, United States

Columbus, Ohio, United States

Oklahoma City, Oklahoma, United States

Philadelphia, Pennsylvania, United States

Pittsburgh, Pennsylvania, United States

Austin, Texas, United States

Dallas, Texas, United States

Houston, Texas, United States

San Antonio, Texas, United States

Los Angeles, California, United States

Toronto, Ontario, Canada

St. John's, Newfoundland And Labrador, Canada

Ottawa, Ontario, Canada

Mississauga, Ontario, Canada

Fountain Valley, California, United States

Miami, Florida, United States

Cherry Hill, New Jersey, United States

Houston, Texas, United States

Medford, Oregon, United States

Englewood, Colorado, United States

Dallas, Texas, United States

Encinitas, California, United States

Colorado Springs, Colorado, United States

Waterbury, Connecticut, United States

Austin, Texas, United States

El Paso, Texas, United States

Gainesville, Florida, United States

Asheville, North Carolina, United States

Elizabeth City, North Carolina, United States

Round Rock, Texas, United States

Scottsdale, Arizona, United States

Bellingham, Washington, United States

Round Lake Beach, Illinois, United States

Oklahoma City, Oklahoma, United States

San Antonio, Texas, United States

Pell City, Alabama, United States

Cypress, California, United States

Mission Hills, California, United States

Centennial, Colorado, United States

Aventura, Florida, United States

Largo, Florida, United States

Ocala, Florida, United States

Tallahassee, Florida, United States

Conyers, Georgia, United States

Lawrenceville, Georgia, United States

Indianapolis, Indiana, United States

Bethesda, Maryland, United States

Brockton, Massachusetts, United States

Forked River, New Jersey, United States

Elizabeth City, North Carolina, United States

Columbus, Ohio, United States

Toledo, Ohio, United States

Okalahoma City, Oklahoma, United States

Oklahoma, Oklahoma, United States

Eugene, Oregon, United States

Lake Oswego, Oregon, United States

Philadelphia, Pennsylvania, United States

Pittsburgh, Pennsylvania, United States

Scranton, Pennsylvania, United States

Mckinney, Texas, United States

Ajax, Ontario, Canada

Mississauga, Ontario, Canada

Ottawa, Ontario, Canada

Point Edward, Ontario, Canada

Sudbury, Ontario, Canada

Toronto, Ontario, Canada

St. Romuald, Quebec, Canada

St. John's, , Canada

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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