Drug Development

Patient enrollment completed in phase III trial for CellCept in myasthenia gravis

Published in Biotech Business Week, December 26th, 2005

Aspreva Pharmaceuticals Corp. (ASPV; ASV) announced completion of enrollment of 176 patients in the phase III clinical study to assess the safety and efficacy of mycophenolate mofetil (MMF or CellCept) to maintain or improve symptom control with reduced corticosteroids in patients with myasthenia gravis (MG).

The randomized, double-blind, placebo-controlled clinical trial is designed to evaluate the efficacy and safety of MMF to maintain or improve symptom control with reduced corticosteroids in patients with myasthenia gravis over a treatment period of 36 weeks. The primary endpoint of responder status in the trial encompasses both minimal disease activity and low...

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Source: Biotech Business Week (2005-12-26)

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