Dr. Ginzler has served on a steering committee (unpaid) and received research funding from Aspreva/Vifor, and has received consulting fees, speaking fees, and/or honoraria from MedImmune, Wyeth, Cephalon, Genentech, Aspreva Pharmaceuticals, Bristol-Myers Squibb, Human Genome Sciences, Merck Serono, Teva Pharmaceuticals, and Zymogenetics (less than $10,000 each), and from the investment analysts Guidepoint Global and Gerson Lehman Group.
Systemic Lupus Erythematosus
Nonrenal disease activity following mycophenolate mofetil or intravenous cyclophosphamide as induction treatment for lupus nephritis: Findings in a multicenter, prospective, randomized, open-label, parallel-group clinical trial†
Version of Record online: 28 DEC 2009
Copyright © 2010 by the American College of Rheumatology
Arthritis & Rheumatism
Volume 62, Issue 1, pages 211–221, January 2010
How to Cite
Ginzler, E. M., Wofsy, D., Isenberg, D., Gordon, C., Lisk, L. and Dooley, M.-A. (2010), Nonrenal disease activity following mycophenolate mofetil or intravenous cyclophosphamide as induction treatment for lupus nephritis: Findings in a multicenter, prospective, randomized, open-label, parallel-group clinical trial. Arthritis & Rheumatism, 62: 211–221. doi: 10.1002/art.25052
ClinicalTrials.gov identifier: NCT00377637. This is protocol WX17801 from the Aspreva Lupus Management Study Group (see Appendix A for principal investigators and study centers).
- Issue online: 28 DEC 2009
- Version of Record online: 28 DEC 2009
- Manuscript Accepted: 25 SEP 2009
- Manuscript Received: 28 JAN 2009
- Aspreva Pharmaceuticals
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