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Riquent(TM) Phase 3 Data Reviewed at EULAR Rheumatology Conference

 

La Jolla Pharmaceutical Company (Nasdaq: LJPC) today announced that Dr. Mario Cardiel, one of its principal investigators, reviewed previously released data from its Phase 3 clinical trial of Riquent(TM) for the treatment of lupus renal disease at the Annual European Congress of Rheumatology "EULAR 2003" in Lisbon, Portugal. His presentation entitled "Randomized, Placebo-controlled, Double-blind, Phase 3 Clinical Trial for the Evaluation of Riquent (LJP 394) in the Treatment of Patients with SLE Who Are at Risk for Renal Flare" was given today.

La Jolla Pharmaceutical Company is a biotechnology company developing therapeutics for antibody-mediated autoimmune diseases afflicting several million people in the United States and Europe. The Company is developing Riquent(TM), formerly known as LJP 394, for the treatment of lupus kidney disease, a leading cause of sickness and death in patients with lupus. The Company is also developing LJP 1082 for the treatment of antibody-mediated thrombosis, a condition in which patients suffer from recurrent stroke, deep- vein thrombosis and other thrombotic events. The Company's common stock is traded on The Nasdaq Stock Market under the symbol LJPC. For more information about the Company, visit its Web site: http://www.ljpc.com/.

 

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