Clinical trials

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Condition / disease
Location
Status: Recruiting

Pharmacodynamic Equivalence of the Test and Reference Metered Dose Inhalers (MDIs) Containing Albuterol Sulfate in Adult Patients With Stable Mild Asthma

The objective of this study is to evaluate the pharmacodynamic (PD) bioequivalence (BE) of albuterol inhalers, test formulation: Albuterol Sulfate HFA inhalation aerosol 108 mcg (equal to albuterol base 90 mcg) per actuation and reference formulation: ProAir HFA (albuterol sulfate) or FDA authorized generic: Albuterol Sulfate HFA (Teva Pharmaceutical USA, Inc.) Inhalation Aerosol 108 mcg (equal to albuterol base 90 mcg) per actuation manufactured by two different manufacturers using methacholine bronchoprovocation challenge test in patients with stable mild asthma.

Participants needed: 148
Trial details
Age: 20-65Biological sex: AllType: InterventionalSponsor: Intech Biopharm Ltd.Updated: Feb 17, 2025Locations: 12
Eligibility criteria

Male, non-pregnant and non-lactating female subjects (20-65 years of age, inclus... [+11]

Evidence of conditions altering airway reactivity to methacholine, including upp... [+18]