Epinephrine Inhalation Aerosol USP: For Evaluation Of Efficacy And Safety In Asthma Patients
Status: | Completed |
---|---|
Conditions: | Asthma |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 12 - 75 |
Updated: | 4/21/2016 |
Start Date: | July 2011 |
End Date: | December 2011 |
Epinephrine Inhalation Aerosol USP, an HFA-MDI: Clinical Study-C For Evaluation Of Efficacy And Safety In Asthma Patients
This clinical study evaluates the 12-week efficacy and safety of Epinephrine HFA Inhalation
Aerosol HFA the proposed HFA formulation of metered dose inhaler (MDI) of Epinephrine, in
comparison to a Placebo-HFA control MDI and the currently marketed Primatene® Mist
(epinephrine CFC inhaler), in adolescent and adult subjects with asthma.
Aerosol HFA the proposed HFA formulation of metered dose inhaler (MDI) of Epinephrine, in
comparison to a Placebo-HFA control MDI and the currently marketed Primatene® Mist
(epinephrine CFC inhaler), in adolescent and adult subjects with asthma.
Inclusion Criteria:
- Patients with documented asthma, requiring inhaled epinephrine or beta 2-agonist
treatment.
- No significant changes in asthma therapy and no asthma-related hospitalization or
emergency visits, within 4 weeks prior to Screening
- Can tolerate withholding treatment with inhaled bronchodilators and other allowed
medications for the minimum washout period.
- Demonstrating a Screening Baseline FEV1 that is 50 - 90% of predicted normal value.
- Demonstrating at least a 12% Airway Reversibility.
- Demonstrating satisfactory techniques in the use of metered-dose inhaler and a hand
held peak expiratory flow meter.
- Female patients of child-bearing potential must be non-pregnant and non-lactating at
Screening and throughout the study, and must use an acceptable method of
contraception during the study.
Exclusion Criteria:
- A smoking history of 10-pack years, or having smoked within 12 months of screening.
- Any current or past medical conditions that, per investigator discretion, might
significantly affect responses to the study drugs, other than asthma.
- Concurrent clinically significant diseases.
- Known intolerance or hypersensitivity to any component of the study drugs.
- Recent infection of the respiratory tract, before screening.
- Use of prohibited medications.
- Having been on other investigational drug/device studies in the last 30 days prior to
screening.
- Known or highly suspected substance abuse.
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