epinephrine inhalation aerosol
DrugEpinephrine inhalation aerosol, 125 mcg/inhalation, 2 inhalations QID at 4 - 6 hour intervals
Other names: epinephrine inhalation aerosol - HFA propelled
NCT Number: NCT01357642
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.
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Notify Me12 year–75 year
All sexes
Interventional
Phase 3
West Coast Clinical Trials, Costa Mesa, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Epinephrine inhalation aerosol, 125 mcg/inhalation, 2 inhalations QID at 4 - 6 hour intervals
Other names: epinephrine inhalation aerosol - HFA propelled
Placebo for epinephrine inhalation aerosol, formulation without epinephrine
Time frame: at 5, 30, 60, 120, 180, 240, and 360 minutes post-dose
Serial FEV1 measurements to demonstrate the mean AUC of change in percent FEV1 from same-day baseline of E004 (Treatment T; Epinephrine-HFA) versus Placebo-HFA (Treatment P) is the primary efficacy endpoint.
Time frame: 2, 10, 20, 60, and 360 min after dosing
Assess blood pressure, pulse rate
Time frame: at baseline, 2, 10, 20, and 60 min post-dose
At study visits 1 and 5 only, perform 12 lead ECG
Time frame: baseline, and at 15 and 120 min post-dose
Monitor blood glucose and potassium levels to assure appropriate balance
Amphastar Pharmaceuticals, Inc.
Industry
Epinephrine Inhalation Aerosol USP, an HFA-MDI: Clinical Study-C For Evaluation Of Efficacy And Safety In Asthma Patients
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View the official ClinicalTrials.gov record (opens in a new tab)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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