U.S., April 12 -- ClinicalTrials.gov registry received information related to the study (NCT06924190) titled 'Pharmacokinetics and Bioequivalence Study of Budesonide Inhalation Aerosol in Humans' on March 29.
Brief Summary: The test formulation of Budesonide Inhalation Aerosol is bioequivalent to the reference formulation in healthy Chinese subjects under fasting conditions.
Study Start Date: Dec. 30, 2024
Study Type: INTERVENTIONAL
Condition:
Bioequivalence Study in Healthy Subjects
Intervention:
DRUG: Budiair(R) 200ug/puff inhalation aerosol
The subjects randomly received one puff Budiair(R)(budesonide inhalation aerosol 200ug/puff )
DRUG: budesonide 200ug/puff inhalation aerosol
The subjects randomly received one puff budesonid...