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Boston Scientific Announces Schedule for ACC 2008
Date:3/25/2008

he ARRIVE program. The

study is designed to capture long-term safety and effectiveness data of

the TAXUS Express2 Stent in more complex patients treated in routine

practice. The results will be presented at 1:54 p.m., during a

moderated e-poster session. The Company plans to issue a press release

at this time.

Monday, March 31

-- PROMUS(TM) and TAXUS Stents. Results from the Spirit II Clinical Trial

will be presented by Patrick W. Serruys, M.D., PhD, at 8:00 a.m.,

during a Late Breaking Trial session in Grand Ballroom S100. Dr.

Serruys will provide a two-year data analysis of 300 patients treated

with the XIENCE(TM) V (PROMUS) Stent or the TAXUS Express Stent.

SPIRIT II is a randomized, non-inferiority trial designed to obtain CE

Mark approval for both the XIENCE V and PROMUS Stents. The PROMUS

Stent is a private-labeled XIENCE V Everolimus-Eluting Coronary Stent

System manufactured by Abbott and distributed by Boston Scientific.

The Company plans to issue a press release at this time.

PROENCY European Registry

In February, Boston Scientific announced the start of its PROENCY

(PROMUS(TM), ENdeavor(R) and CYpher(R)) European registry, which is

the first of its kind to observe different 'olimus'-eluting coronary

stents. The study will collect real-life clinical outcome data for

Boston Scientific's PROMUS Everolimus-Eluting Stent and compare them

with data from Johnson & Johnson's Cypher(R) Sirolimus-Eluting Stent

and Medtronic's Endeavor(R) Zotarolimus-Eluting Stent in patients

treated in routine clinical practice. Clinical investigators are

currently being recruited for the U.S. phase of PROENCY, which will

begin upon U.S. launch of the PROMUS Stent expected later this year.

-- Biventricular Pacing Percentage in Heart
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SOURCE Boston Scientific Corporation
Copyright©2008 PR Newswire.
All rights reserved

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