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Mar12
La Jolla Pharmaceutical’s Riquent® Passed Interim Phase 3 Trial in Lupus Patients
Interim clinical data of La Jolla Pharmaceutical Company (Nasdaq: LJPC)’s ongoing double-blind, placebo-controlled randomized Lupus Phase 3 trial of Riquent® (abetimus sodium) revealed positive antibody results.

Analyses of interim antibody data indicate that patients treated with 900 mg or 300 mg per week doses of Riquent had greater reductions in antibodies to double-stranded DNA (dsDNA) than patients treated with la_jolla.gif100 mg per week or placebo.

The results showed a significant dose response when comparing all Riquent-treated patients to placebo-treated patients (p < 0.0001), and each Riquent dose group to the placebo dose group (p < 0.0015 for 100 mg, p < 0.0001 for 300 mg and 900 mg).

Riquent® (abetimus sodium) is La Jolla Pharmaceutical Company’s drug candidate for systemic lupus erythematosus (lupus or SLE) - a chronic, potentially life-threatening autoimmune disease.

Read the full report.


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« Supplemental New Drug Application (sNDA) for Pediatric Doses of Tamiflu®, Submitted by Roche to USFDA | Main | Oxford BioMedical Will Acquire Oxxon Therapeutics »

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