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EMBARGOED FOR RELEASE
March 12, 2000
Time of Presentation
or News Conference (PST)
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Contact: Melanie Caudron or Beth Cassady
March 12-15: 714-765-2021
After March 15: 301-897-2628
(not for publication) |
ACC
49th Annual Scientific Session
Late-Breaking Clinical Trials
in Interventional Cardiology (#72)
Tuesday, March 14, 2000 (8:30 a.m.-10:00 a.m.)
(ANAHEIM, CALIF.)—Clots that cause heart attacks by
blocking coronary arteries can be dissolved with thrombolytic
agents, the so-called clot busters. The anticoagulant
heparin is often given along with the clot-busting drug
to help restore and maintain blood flow to the heart
muscle. But because heparin has a number of limitations
that make it hard to use in many patients, physicians
have long been searching for better alternatives. A
study has tested whether a recently developed synthetic
pentasaccharide agent might be superior to heparin in
patients who receive the clot buster t-PA for a heart
attack.
In the PENTALYSE trial, 333 patients receiving t-PA
were randomized to receive either heparin or the synthetic
pentasaccharide agent at one of three dosages. The pentasaccharide
works like an anticoagulant by inhibiting the biochemical
action of activated factor X, a key molecule involved
in clot formation.
The study was designed to show whether the synthetic
anticoagulant is safe and as effective as heparin at
preventing recurrent angina, heart attacks, and other
events that returning intracoronary clots can cause.
Patients in the study were followed for 30 days.
Dr. Frans Van de Werf, of University Hospital Gasthuisberg
in Leuven, Belgium, will present the results of the
PENTALYSE trial on Tuesday, March 14, at 8:30 a.m. at
the American College of Cardiology 49th Annual Scientific
Session in Anaheim, Calif.
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