Drug intelligence / Profile preview

Esprit BTK Everolimus Eluting Resorbable Scaffold System

Development stage
Unknown
Lead developer
Abbott
Modality
Small Molecules, Implantable Devices → Device-based Delivery → Drug Delivery Systems
Administration
Intra-arterial, Percutaneous, Implant
01

Overview

The Esprit BTK Everolimus Eluting Resorbable Scaffold System is a first-in-class, FDA-approved drug-eluting resorbable scaffold designed for the treatment of chronic limb-threatening ischemia (CLTI) in patients with below-the-knee (BTK) peripheral arterial disease. The device consists of an absorbable mesh tube that is coated with everolimus and implanted into narrowed arteries in the lower leg to restore blood flow and prevent vessel re-narrowing. Unlike permanent metal stents, the scaffold provides temporary mechanical support while gradually releasing everolimus to inhibit neointimal hyperplasia and then fully resorbs over time. The mechanism of action involves local delivery of everolimus, which inhibits growth factor-stimulated cell proliferation by forming a complex with FKBP-12 and interfering with mTOR signaling, leading to cell cycle arrest at late G1 phase. Clinical trials have demonstrated superior efficacy compared to balloon angioplasty alone in maintaining vessel patency and reducing major adverse limb events[2][3][4][5][6][8].

Brand names
Esprit BTK
Other names
Esprit BTK Resorbable Scaffold SystemEsprit BTK Everolimus Eluting Resorbable Scaffold SystemEsprit™ BTK
02

Targets

Mechanistic target of rapamycin complex 1

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