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OpenTrials
Completed

NCT Number: NCT00393952

New Combination Inhaler (FlutiForm HFA MDI 100/10 µg and 250/10 µg) Versus Fluticasone and Formoterol Administered Alone, and Placebo in Patients With Moderate to Severe Asthma

The purpose of this study is to compare the efficacy and safety of the fixed combination asthma drug FlutiForm with its two components administered alone, fluticasone propionate and formoterol fumarate, and with placebo in adult and adolescent patients with moderate to severe asthma.

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Key information

Age range

12 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Research Center, Ponce, Puerto Rico

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Ages eligible for study: 12 years and above; genders eligible for study: both; prior steroid use: steroid-requiring

Inclusion criteria

  • History of asthma for at least 12 months.
  • Documented use of inhaled corticosteroid for at least 4 weeks prior to Screening Visit Demonstrate FEV-1 of 40-80% of predicted normal values at Screening and Baseline Visit.
  • Documented reversibility of 15% within 12 months of Screening visit 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.

Treatment and study plan

Fluticasone propionate/Formoterol fumarate 250/10

Drug

FlutiForm 250/10ug is a HFA pMDI that delivers 125ug of Fluticasone propionate per actuation and 5ug of Formoterol fumarate per actuation. Patients will take 2 actuations BID for 12 weeks.

Other names: FlutiForm 250/10

Placebo

Drug

Placebo is a HFA pMDI that delivers placebo aerosol. Patients will take 2 actuations BID for 12 weeks.

Other names: SKP Placebo

Fluticasone propionate/formoterol fumarate 100/10

Drug

FlutiForm 100/10ug is a HFA pMDI that delivers 50ug of Fluticasone propionate per actuation and 5ug of Formoterol fumarate per actuation. Patients will take 2 actuations BID for 12 weeks.

Other names: FlutiForm 100/10

Fluticasone propionate 250

Drug

Fluticasone 250 is a HFA pMDI that delivers 125ug of Fluticasone propionate per actuation. Patients will take 2 actuations BID for 12 weeks.

Other names: Fluticasone 250

Formoterol fumarate 10

Drug

Formoterol 10ug is a HFA pMDI that delivers 5ug of Formoterol fumarate per actuation. Patients will take 2 actuations BID for 12 weeks.

Other names: SKP Formoterol 10

Primary outcomes

  1. Change in Forced Expiratory Volume in 1 s(FEV-1) from Baseline (Week 0) to Week 12.

    Time frame: Week 0 and 12 visits

  2. Discontinuation due to lack of efficacy.

    Time frame: Whole duration of study

Secondary outcomes

  1. Other pulmonary function tests including forced vial capacity (FVC) and peak expiratory flow rate (PEFR).

    Time frame: Whole duration of study

  2. Clinical endpoints (frequency of asthma exacerbations and patient data captured in diary including daily morning and evening PEFR).

    Time frame: Whole duration of study

  3. Serial 12-hour FEV-1 area under the curve (AUC).

    Time frame: Week 0, 2 and 12 visits

  4. Safety variables including adverse events, ECGs clinical laboratory tests and vital signs.

    Time frame: Whole duration of study

Sponsors and collaborators

Lead sponsor

SkyePharma AG

Industry

Registry information

Official study title

A Randomized, Double-blind, Placebo-controlled, Parallel Group, Stratified, Multi-center, 12-Week Study Comparing the Safety and Efficacy of Fluticasone and Formoterol Combination (FlutiForm(tm) 100/10 µg or 250/10 µg Twice Daily) in a Single Inhaler (SkyePharma HFA pMDI) With the Administration of Placebo or Fluticasone (250 µg Twice Daily) and Formoterol (10 µg Twice Daily) Alone in Adolescent and Adult Patients With Moderate to Severe Asthma

Important dates

Study start
2006
Primary completion
2008
Study completion
2008
First posted
Oct 31, 2006
Registry last updated
Jun 23, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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