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PentaLyte®
STATUS: PHASE I TRIAL COMPLETED |
BLOOD PLASMA VOLUME EXPANSION CARDIOPULMONARY BYPASS SURGERY |
NEW PRODUCT DEVELOPMENTS
BioTime Successfully Completes PentaLyte Phase I Clinical Trial (8/30/00)
BioTime to Begin Clinical Studies of PentaLyte (4/18/00)
BioTime, Inc. announced on June 15, 1998 that in a laboratory study in
rabbits, PentaLyte® substantially improved protection of the stomach and
lung from damage in the treatment of hypovolemia. PentaLyte®, currently in
preparation for clinical trials, was compared to Ringer's lactate - the
crystalloid most often employed in surgical procedures. The research was
conducted by a team led by Dr. Vance G. Nielsen of the Department of
Anesthesiology at the University of Alabama at Birmingham, one of the
nation's leading centers for cardiac surgery. The study is published in
the June issue of the American Journal of Respiratory and Critical Care
Medicine (Am J Respir Crit Care Med Vol 157, pp 1982-1990, 1998). Reprints
of the report will be available from BioTime and can be found on the
Internet at http://www.ajrccm.org.
PRODUCT DESCRIPTION
PentaLyte is BioTime's proprietary pentastarch-based synthetic plasma expander, designed especially for use when a faster elimination of the starch component is desired and acceptable. Of the approximately 10,000,000 surgeries that occur within U.S. hospitals each year, about 25% require blood transfusions. A substantial portion of the remaining surgeries, while not requiring transfusions, do cause blood loss. In addition, many patients are treated for injuries that result in significant bleeding. Although Hextend can be used in these cases, some physicians appear to prefer a solution which could be metabolized faster and excreted earlier when the longer term protection provided by Hextend is not required. PentaLyte combines the physiologically balanced Hextend formulation with pentastarch, a medical starch currently available in the U.S., with a lower molecular weight and degree of substitution (see diagram below) than the hetastarch used in Hextend. By testing and bringing both Hextend and PentaLyte to the market, BioTime can increase its market share by providing the medical community with solutions to match patients' needs.

PentaLyte® is a solution almost identical to Hextend® but containing a lower molecular weight starch (called pentastarch) which is substituted with fewer hydroxyethyl groups. Its lower molecular weight and degree of substitution results in its removal from the blood more rapidly than hetastarch.
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BioTime, Inc. 1301 Harbor Bay Pkwy Alameda, CA 94502 tel: 510.521.3390 fax: 510.521.3389
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© 2007 BioTime, Inc. | All Rights Reserved. |
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