Safety and Efficacy of GENOSS® DCB With a Shellac Plus Vitamin E Excipient in Patients With De Novo Lesion
NCT07158307 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 3000
Last updated 2025-09-05
Summary
The GENOSS PCB-De Novo study aims to evaluate the long-term efficacy and safety of a paclitaxel-coated balloon catheter containing shellac and vitamin E excipients (Genoss® DCB) in patients with De novo small coronary artery disease.
Conditions
- Coronary Artery Disease(CAD)
Sponsors & Collaborators
-
Genoss Co., Ltd.
lead INDUSTRY
Eligibility
- Min Age
- 19 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-06-27
- Primary Completion
- 2030-06-27
- Completion
- 2031-06-30
Countries
- South Korea
Study Locations
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