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A Randomized, Safety and Efficacy Study of Taneasy 600mg Granules and Actein Effervescent Tablets 600MG in COPD Subjects
To evaluate the safety and efficacy of Taneasy 600mg granules and Actein effervescent tablets 600MG administered twice daily for 14 days in treatment of COPD Disease.
The study will enroll 40\~60 patients and complete 40 patients.
Age
20 - 75 years
Sex
ALL
Healthy Volunteers
No
Taichung Veterans General Hospital
Taichung, Taiwan
Start Date
September 20, 2024
Primary Completion Date
December 31, 2024
Completion Date
December 31, 2024
Last Updated
February 5, 2025
42
ACTUAL participants
Taneasy 600mg granules
DRUG
Actein effervescent 600mg
DRUG
Lead Sponsor
Bun Yao Biotechnology Co., Ltd
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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View ClinicalTrials.gov Terms and ConditionsNCT06958666