_COMPANY

Myasthenia gravis (MG)


Vifor Pharma partner: F. Hoffmann-La Roche Ltd

Product name: CellCept

Generic name: Mycophenolate Mofetil (MMF)

Approved indications: The prevention of rejection of kidney, heart and liver transplants.

Clinical study summary: Randomized, double-blind placebo controlled clinical trial designed to investigate the efficacy and safety of CellCept for patients with myasthenia gravis over a treatment period over 36 weeks.

Primary endpoint: The primary endpoint of responder status encompasses both minimal disease activity and low steroid dose.

Phase of development: Phase III

Trial initiation (first patient enrolled): April 2004

Trial complete: failed to meet both primary and secondary endpoints.



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