Pharmacokinetics and Bioequivalence Study of Budesonide Inhalation Aerosol in Humans

NACompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

December 30, 2024

Primary Completion Date

January 20, 2025

Study Completion Date

January 20, 2025

Conditions
Bioequivalence Study in Healthy Subjects
Interventions
DRUG

Budiair® 200ug/puff inhalation aerosol

The subjects randomly received one puff Budiair®(budesonide inhalation aerosol 200ug/puff )

DRUG

budesonide 200ug/puff inhalation aerosol

The subjects randomly received one puff budesonide inhalation aerosol(200ug/puff )

Trial Locations (2)

214000

Wuxi People's Hospital, Wuxi

276002

Lunan Better Pharmaceutical Co., Ltd., Linyi

All Listed Sponsors
collaborator

Wuxi People's Hospital

OTHER

lead

Lunan Better Pharmaceutical Co., LTD.

INDUSTRY

NCT06924190 - Pharmacokinetics and Bioequivalence Study of Budesonide Inhalation Aerosol in Humans | Biotech Hunter | Biotech Hunter