drugset / Trial / NCT00542763

Mycophenolate Sodium Treatment in Patients With Primary Sjogren's Syndrome

NCT00542763

Phase 1 Completed 12 enrolled University Hospital Muenster Novartis · collab
NaSingle-groupOpen-labelTreatment

Summary

Primary Sjogren's syndrome (pSS) is an autoimmune disorder characterized by keratoconjunctivitis sicca and xerostomia. In addition, various extraglandular manifestations may develop. Several immunomodulating agents have been attempted in the treatment of pSS without achieving satisfactory results. Currently, there is no approved systemic treatment for pSS. Mycophenolic acid (MPA) is a selective inhibitor of inosine-monophosphate-dehydrogenase which leads to inhibition of the de novo pathway of nucleotide synthesis. The antiproliferative effect of MPA mainly affects activated T- and B-lymphocytes because the proliferation of these cells is critically dependent on the de novo purine synthesis compared to other eukaryotic cells. Since these lymphocytes have been suggested to play a pivotal role in the inflammation and immunopathogenesis of pSS, mycophenolate-sodium might be a promising agent in the treatment of pSS. We perform a single-centre, open-label pilot trial with Mycophenolate sodium in pSS.

Timeline

Start
2005-04
Primary completion
Completion
2007-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Mycophenolate Sodium Unknown 720 mg Oral
Subject Mycophenolate Sodium Unknown 1440 mg Oral

Indications