Asthma Clinical Trial
Official title:
Randomized, Single-dose, Three-way Crossover Study to Assess the Bioavailability of Using SYN006 HFA MDI (Budesonide/Procaterol 180/10mcg) vs Pulmicort pMDI (Budesonide 200 μg) and Meptin Air (Procaterol 10mcg)" in Healthy Volunteer.
Budesonide + Procaterol HFA MDI is a novel asthma product containing both budesonide and procaterol in a single inhaler. Budesonide is a corticosteroid that treats underlying airway inflammation in asthma. Procaterol is a direct acting sympathomimetic with predominantly Beta-adrenoceptor stimulant activity selective to Beta-2 receptors (a Beta-2 agonist). It is used as a bronchodilator in the management of reversible airways obstructive pulmonary disease. Budesonide and Procaterol therefore have complementary effects, treating two different components of asthma.
Test drug : SYN006 HFA MDI (Budesonide + Procaterol Hydrochloride) Strength: (Budesonide
180ug and Procaterol Hydrochloride 10ug/puff) Mode of administration: Orally inhaled
administration, single dose (4 puffs)
Reference drug 1 : Pulmicort pMDI (Budesonide) Strength: (Budesonide 200ug/puff) Mode of
administration: Orally inhaled administration, single dose (4 puffs)
Reference drug 2 : Meptin Air 10ug (Procaterol Hydrochloride) Strength: (Procaterol
Hydrochloride 10ug/puff) Mode of administration: Orally inhaled administration, single dose
(4 puffs)
One dose for each drug (Test, Reference 1 and Reference 2)with an at least 6-day washout
period.
;
Allocation: Randomized, Endpoint Classification: Bio-availability Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
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