Treatment of SFA lesions with Drug-Eluting technologies

SUSTAINED RELEASE – SUPERIOR RESULTS

Eluvia demonstrated Superior Results in the World’s First Head-to-Head DES SFA Trial. Eluvia is the first and only SFA technology that sustains drug release beyond one year.
Cirse Imperial animation Post Data Release
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The Growing Evidence Base on Drug Eluting Technologies: A new Focus on Drug Eluting Stent 

New focus on drug eluting stent
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  • Results of the IMPERIAL Randomized Controlled Trial of Eluvia vs Zilver PTX
  • Drug Eluting Stent in Peripheral Artery Disease, Critical Limb Ischemia and Below The Knee indications 

Boston Scientific is the only company investing in a complete portfolio of drug-eluting therapies, designed to revolutionize the field, as well as ground-breaking pre-clinical and clinical research that are helping define how to better use the technologies. Our commitment is to bring forward innovative therapies that can make a difference in the lives of patients, and our foundation of more than 15 years of design and development has established our clinical leadership.

Eluvia Data Sheet
Data sheet

IMPERIAL datasheet (DES SFA)

Eluvia Data Sheet
Data sheet

Ranger All-Comers Registry 12 Month-data

Did you know

DID YOU KNOW

Boston Scientific is the only company investing in a complete portfolio of Drug-Eluting Therapies.
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Products Overview

ELUVIATM Drug-Eluting
Vascular Stent System

The Eluvia Drug-Eluting Stent delivers unprecedented results in the SFA through its unique SUSTEND™ drug-delivery
technology.
MAJESTIC Trial

RANGERTM Paclitaxel-Coated
PTA Balloon Catheter

The Ranger Drug Coated balloon has been designed to provide consistent and predictable drug delivery through efficient drug transfer and a strong coating integrity.
RANGER SFA RCT
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RANGER™ - New long lenghts.

RANGER™ Product information

Disclaimer
1. Superiority determined in Post Hoc Superiority Analysis (Continuity Adjusted Chi-Square p-value). Primary patency rate of 86.8% in the Eluvia arm vs. 77.5% in the Zilver PTX arm (p-value = 0.0210). Major adverse event rate of 4.9% in the Eluvia arm vs. 9.0% in the Zilver PTX arm (p-value = 0.0975). Primary patency defined as PSVR ≤ 2.5 without a hemodynamically significant stenosis on duplex ultrasound and without clinically-driven TLR or bypass of the target lesion.

CAUTION: The law restricts these devices to sale by or on the order of a physician. Indications, contraindications, warnings and instructions for use can be found in the product labelling supplied with each device. Information for use only in countries with applicable health authority registrations. Material not intended for use in France. 2017 Copyright © Boston Scientific Corporation or its affiliates. All rights reserved.

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