Study of Mometasone Furoate/Formoterol Combination and Fluticasone/Salmeterol in Persistent Asthmatics Previously Treated With Inhaled Glucocorticosteroids (P04139)

Inclusion criteria

• Subjects of either sex and any race, at least 12 years of age, with a diagnosis of asthma of at least 12 months.
• Use of medium or high daily dose of ICS (alone or in combination with long-acting beta-agonist [LABA]) for at least 12 weeks prior to Screening and have been on a stable regimen for at least 2 weeks prior to Screening.

• Medium daily doses of ICS:

• > 500 to 1000 mcg beclomethasone chlorofluorocarbon (CFC)
• > 250 to 500 mcg beclomethasone hydrofluoroalkane (HFA)
• > 600 to 1000 mcg budesonide dry powder inhaler (DPI)
• > 1000 to 2000 mcg flunisolide
• > 250 to 500 mcg fluticasone
• 400 mcg MF
• > 1000 to 2000 mcg triamcinolone acetonide
• High daily doses of ICS:

• > 1000 mcg beclomethasone CFC
• > 500 mcg beclomethasone HFA
• > 1000 mcg budesonide DPI
• > 2000 mcg flunisolide
• > 500 mcg fluticasone
• > 400 mcg MF
• > 2000 mcg triamcinolone acetonide
• If there is no inherent harm in changing the subject's current asthma therapy, the subject must discontinue prescribed ICS or ICS/LABA combination at Baseline.
• Must show evidence of reversibility within the last 12 months or during the Screening Period. Historical reversibility defined as an increase in absolute forced expiratory volume in 1 second (FEV1) of >= 12% and >= 200 mL will qualify if performed within 12 months of Screening. If no historical reversibility, subject must demonstrate an absolute FEV1 of >= 12% and >= 200 mL within 10 to 15 minutes after four puffs of salbutamol at Visit 1 or anytime prior to Baseline.
• At Screening and Baseline, FEV1 must be >= 50% predicted, when restricted medications are withheld for the appropriate intervals.
• Complete blood count, blood chemistries, urinalysis, and electrocardiogram (ECG) conducted at Screening must be within normal limits or clinically acceptable to the investigator/sponsor. A chest x-ray performed at Screening or within 12 months prior must be clinically acceptable.
• A female of childbearing potential must be using a medically acceptable, adequate form of birth control:

• prescribed hormonal contraceptives;
• medically prescribed intrauterine device (IUD);
• medically prescribed transdermal contraceptive;
• condom in combination with spermicide;
• monogamous relationship with a male partner who has had a vasectomy.

Birth control must have started at least 3 months prior to Screening. Subject must agree to continue its use for the duration of the study. A subject of childbearing potential who is not currently sexually active must agree to use a medically acceptable method should she become sexually active during the study. Women who have been surgically sterilized or are at least 1 year postmenopausal are not considered to be of childbearing potential. A subject of childbearing potential must have a negative serum pregnancy test at Screening.

Key Exclusion Criteria:

• A change (increase or decrease) in absolute FEV1 of > 20% at any time from the Screening Visit up to, and including, the Baseline Visit.
• A subject who requires the use of > 12 inhalations per day of short-acting beta-agonist (SABA) MDI or > 2 nebulized treatments per day of 2.5 mg salbutamol, on any 2 consecutive days from the Screening Visit up to, and including, the Baseline Visit.
• A subject who experiences a clinical asthma exacerbation (defined as a deterioration of asthma that results in emergency treatment, hospitalization due to asthma, or treatment with additional, excluded asthma medication [other than SABA]) at any time from the Screening Visit up to, and including, the Baseline Visit.
• A subject who has ever required ventilator support for respiratory failure secondary to asthma.
• A subject who is a smoker or ex-smoker and has smoked within the previous year or has had a cumulative smoking history > 10 pack-years.