Non-inferiority Clinical Trial to Compare the Safety and Performance of MeRes100 Sirolimus-eluting BioResorbable Vascular Scaffold System Versus Contemporary DES Platforms in Patients With de Novo Coronary Artery Lesions
Stopped Operational and feasibility constraints due to regulatory requirements
Conditions
Interventions
- DEVICE: MeRes 100 Sirolimus-eluting Bioresorbable Vascular Scaffold System (BRS)
Sponsor
Meril Life Sciences Pvt. Ltd.