Mehling, Matthias and Kappos, Ludwig and Derfuss, Tobias. (2011) Fingolimod for multiple sclerosis : mechanism of action, clinical outcomes, and future directions. Current neurology and neuroscience reports, Vol. 11, no. 5. pp. 492-797.
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Official URL: http://edoc.unibas.ch/dok/A6007321
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Abstract
The oral sphingosine 1-phosphate receptor (S1PR) modulator fingolimod functionally antagonizes S1PR hereby blocking lymphocyte egress from secondary lymphoid organs to the peripheral blood circulation. This results in a reduction in peripheral lymphocyte counts, including potentially encephalitogenic T cells. In patients with relapsing multiple sclerosis fingolimod has been shown to be an effective treatment. In phase 2 and phase 3 studies fingolimod-treated patients had reduced disease activity clinically and in MRI. Although severe infectious complications occurred in single cases treated with fingolimod, the frequency of overall infections was comparable in fingolimod-treated patients and controls. Overall, in clinical studies fingolimod was well tolerated and had a favorable safety profile. In follow-up studies with continuous fingolimod, treatment showed sustained efficacy while being well tolerated.
Faculties and Departments: | 03 Faculty of Medicine > Bereich Medizinische Fächer (Klinik) > Neurologie > Neuroimmunologie (Kappos) 03 Faculty of Medicine > Departement Klinische Forschung > Bereich Medizinische Fächer (Klinik) > Neurologie > Neuroimmunologie (Kappos) 03 Faculty of Medicine > Bereich Medizinische Fächer (Klinik) > Neurologie > Molekulare Neuroimmunologie (Derfuss) 03 Faculty of Medicine > Departement Klinische Forschung > Bereich Medizinische Fächer (Klinik) > Neurologie > Molekulare Neuroimmunologie (Derfuss) |
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UniBasel Contributors: | Kappos, Ludwig and Derfuss, Tobias Johannes |
Item Type: | Article, refereed |
Article Subtype: | Book Review |
Publisher: | Current Science Inc. |
Note: | Publication type according to Uni Basel Research Database: Journal item |
Last Modified: | 26 Apr 2013 07:03 |
Deposited On: | 26 Apr 2013 07:01 |
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