Amphastar Study Site 1
Cypress, California, 90630, United States
NCT Number: NCT01255709
This study examines the pharmacokinetic profile of Armstrong's proposed Epinephrine Inhalation Aerosol USP, an HFA134a propelled Metered Dose Inhaler (MDI) (E004), using a stable isotope deuterium-labeled epinephrine (epinephrine-d3) to differentiate the administered drug from the endogenous epinephrine, in healthy male and female adult volunteers.
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Notify Me18 year–30 year
All sexes
Interventional
Phase 2
Cypress, California, 90630, United States
The current study is designed to complement and expand the previous PK studies, API-E004-CL-B and API-E004-CL-B2, with emphasis on lower E004 dose strengths (at 90 and 100 mcg per inhalation), for a more thorough evaluation of the E004 PK profiles. Safety of E004 will also be evaluated, under augmented dose conditions.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
epinephrine inhalation aerosol, 90 mcg/inhalation, 12 inhalations over 6 minutes
Other names: epinephrine inhalation aerosol
epinephrine inhalation aerosol, 100 mcg/inhalation, 12 inhalations over 6 minutes
Other names: epinephrine inhalation aerosol
epinephrine inhalation aerosol, 220 mcg/inhalation, 12 inhalations over 6 minutes
Other names: epinephrine inhalation aerosol
Time frame: -30, 2, 5, 7.5, 10, 12.5, 15, 20, 25, 30, 45, 60, 90, 120, 240 and 360 min postdose.
Samples will be analyzed with an established LC/MS/MS method, with a quantitative detection limit of 0.02 ng/mL, for both epinephrine-d3 and epinephrine-h3.
Time frame: within 30 min predose, at 30, 60 and 360 min postdose
Systolic and Diastolic Blood pressure and heart rate
Time frame: within 30 min pre-dose, and at 15 and 120 min post-dose
12 lead ECG (Routine and QT/QTc intervals)
Time frame: within 30 min pre-dose, and during the initial 5 min post-dose
Telemetry recording of heart rate
Amphastar Pharmaceuticals, Inc.
Industry
CLINICAL STUDY-B3 FOR ASSESSMENT OF PHARMACOKINETICS, A Randomized, Evaluator-Blind, Single-Dose, Three Arm, Crossover,PK Study in Healthy Volunteers
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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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