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Trial information

A Continuation Study to Assess the Effect of CellCept in Patients With Myasthenia Gravis.

Status: No longer recruiting

Protocol number: WX18411

Sponsor: Hoffmann-La Roche; Aspreva Pharmaceuticals Corporation

Company division: Pharmaceutical

Official Scientific Title: A randomized, double-blind study to evaluate the safety of continued treatment with CellCept in patients with well-controlled myasthenia gravis receiving a stable dose of prednisone

Brief summary: This 2 arm study will provide optional continuation of double-blind treatment with CellCept or placebo, in patients with myasthenia gravis who have achieved good symptom control in study WX17798. Patients who have completed 36 weeks of treatment in study WX17798, with stable prednisone dosing for the last 4 weeks, can continue on blinded treatment with CellCept (1g bid) or placebo until the database for WX17798 is locked and unblinded. The anticipated time on study treatment is 3-12 months, and the target sample size is 100-500 individuals. Target sample size is 136.

Study phase: III

Study type: Interventional; Treatment; Randomized; Double Blind; Placebo; Parallel; Safety/Efficacy study

Condition: Myasthenia Gravis generalised

Intervention type: Drug

Intervention name: mycophenolate mofetil [CellCept]

Primary outcome: 1. AEs, laboratory parameters, vital signs. Time frame: Throughout study

Key secondary outcomes: 1. None Time frame: None

Inclusion criteria:

  • subjects who have completed 36 weeks of treatment in study WX17798, and who have demonstrated good symptom control with a stable prednisone dose for the final 4 weeks of that study.

Exclusion criteria:

  • regularly scheduled plasma exchange or intravenous immunoglobulin treatment;
  • medical condition, adverse event or intolerance of double-blind treatment which would preclude continuation.

Gender: Males or Females

Age limits: Min: 18 Years Max: 80 Years

Accepts healthy volunteers: No

Trial registration date: 09/18/2006

Date last updated: 8/19/2008


Link to trial result

This trial was conducted at the following locations:

Germany

  • München
  • Regensburg

Italy

  • Milano
  • Roma

Ukraine

  • Kharkov
  • Kiev

United Kingdom

  • Liverpool
  • Oxford
  • Salford

United States

  • Sacramento, CA
  • Upland, PA

To contact Roche for more information on this trial please complete the email form below. Treatment decisions and/or suitability for a specific trial are decisions only your healthcare provider can make. If you are patient interested in any of the studies, please have your healthcare provider contact us via this website, and they will be provided with the relevant clinical trial information.

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