Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
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].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Esprit BTK Everolimus Eluting Resorbable Scaffold System.