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Strategies & Market Trends : The 56 Point TA; Charts With an Attitude

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To: Doug R who wrote (31990)9/14/1999 9:15:00 AM
From: John Miz  Read Replies (1) of 79214
 
ALLP NEWS>
biz.yahoo.com

SAN DIEGO--(BW HealthWire)--Sept. 14, 1999--Alliance Pharmaceutical Corp. (Nasdaq:ALLP - news)
announced today that it has reached agreement with the Food and Drug Administration (FDA) on the key
design features of the Phase 3 program for Oxygent(TM), an intravascular oxygen carrier (''blood
substitute'') intended to reduce the need for donor blood transfusions in surgical patients.

Oxygent will be studied in a Phase 3 clinical (human) trial in the U.S. involving patients undergoing
coronary artery bypass grafting (CABG) surgery under cardiopulmonary bypass (CPB). This study, which
is expected to start shortly, will complement a Phase 3 trial currently underway with general surgery
patients in eight European countries. Oxygent is the only blood substitute in clinical development that is
formulated from a synthetic raw material (emulsified perflubron) and not derived from human or bovine
blood.
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