Viewing Study NCT06688292


Ignite Creation Date: 2025-12-24 @ 3:17 PM
Ignite Modification Date: 2026-02-21 @ 10:11 PM
Study NCT ID: NCT06688292
Status: COMPLETED
Last Update Posted: 2025-02-05
First Post: 2024-11-11
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: The Safety and Effectiveness of Taneasy and Actein in COPD Patients
Sponsor: Bun Yao Biotechnology Co., Ltd
Organization:

Study Overview

Official Title: A Randomized, Safety and Efficacy Study of Taneasy 600mg Granules and Actein Effervescent Tablets 600MG in COPD Subjects
Status: COMPLETED
Status Verified Date: 2024-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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.
Detailed Description: The study will enroll 40\~60 patients and complete 40 patients.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: