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

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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.


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.
We found this trial at
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Seattle, Washington 98105
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Ashland, Oregon 97520
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Bellevue, Nebraska 68123
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Bozeman, Montana 59718
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Centennial, Colorado 80112
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Charleston, SC
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Cincinnati, Ohio 45242
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Costa Mesa, California 92626
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Denver, CO
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El Paso, Texas 79903
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Eugene, Oregon 97401
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Iowa City, Iowa 52240
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Lake Oswego, OR
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Los Angeles, CA
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Louisville, KY
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Medford, OR
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Minneapolis, Minnesota 55402
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New Braunfels, Texas 78130
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No. Dartmouth, Massachusetts 02747
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Orange, CA
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Pittsburg, Pennsylvania 15241
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Plymouth, Minnesota 55441
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Portland, Oregon 97213
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Raleigh, North Carolina 27607
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Richmond, Virginia 23229
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San Antonio, Texas 78229
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Skillman, New Jersey 08558
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Upland, Pennsylvania 19013
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Wheat Ridge, Colorado 80033
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Woodstock, Georgia 30188
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