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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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