Current and Emerging Therapies for the Treatment of Multiple Sclerosis: Focus on Cladribine

Multiple Sclerosis (MS) is a chronic inflammatory, immune-mediated, demyelinating disorder of the central nervous system with a heterogeneous clinical presentation and pathology in which activated lymphocytes play an important role in mediating tissue damage. Until recently, all first line therapies...

Full description

Bibliographic Details
Main Authors: Teri L. Schreiner, Augusto Miravalle
Format: Article
Language:English
Published: SAGE Publishing 2012-04-01
Series:Journal of Central Nervous System Disease
Online Access:https://doi.org/10.4137/JCNSD.S5128
id doaj-eea1c6e91b084c088f898b04e057dfcb
record_format Article
spelling doaj-eea1c6e91b084c088f898b04e057dfcb2020-11-25T03:40:12ZengSAGE PublishingJournal of Central Nervous System Disease1179-57352012-04-01410.4137/JCNSD.S5128Current and Emerging Therapies for the Treatment of Multiple Sclerosis: Focus on CladribineTeri L. Schreiner0Augusto Miravalle1Department of Neurology, University of Colorado, Denver, CO, USA.Department of Neurology, University of Colorado, Denver, CO, USA.Multiple Sclerosis (MS) is a chronic inflammatory, immune-mediated, demyelinating disorder of the central nervous system with a heterogeneous clinical presentation and pathology in which activated lymphocytes play an important role in mediating tissue damage. Until recently, all first line therapies for MS were injectable. Several oral medications have been studied for preventative treatment of MS. Cladribine (2-chlorodeoxyadenosine) is a purine nucleoside analog that has been used for the treatment of several hematologic neoplasms, with a unique lymphcytotoxic mechanism of action. Cladribine has been investigated as treatment of MS for more than 15 years. A recent placebo-controlled, double-blind study of cladribine, CLARITY, showed decreased relapse rates, risk of disability progression and MRI measures of disease activity at 96 weeks. Cladribine's strengths included high efficacy and convenient, biannual oral dosing. However, concerns about safety prevented the FDA from approving cladribine in 2011. Thus, use of cladribine for treatment of relapsing and remitting multiple sclerosis will remain off-label.https://doi.org/10.4137/JCNSD.S5128
collection DOAJ
language English
format Article
sources DOAJ
author Teri L. Schreiner
Augusto Miravalle
spellingShingle Teri L. Schreiner
Augusto Miravalle
Current and Emerging Therapies for the Treatment of Multiple Sclerosis: Focus on Cladribine
Journal of Central Nervous System Disease
author_facet Teri L. Schreiner
Augusto Miravalle
author_sort Teri L. Schreiner
title Current and Emerging Therapies for the Treatment of Multiple Sclerosis: Focus on Cladribine
title_short Current and Emerging Therapies for the Treatment of Multiple Sclerosis: Focus on Cladribine
title_full Current and Emerging Therapies for the Treatment of Multiple Sclerosis: Focus on Cladribine
title_fullStr Current and Emerging Therapies for the Treatment of Multiple Sclerosis: Focus on Cladribine
title_full_unstemmed Current and Emerging Therapies for the Treatment of Multiple Sclerosis: Focus on Cladribine
title_sort current and emerging therapies for the treatment of multiple sclerosis: focus on cladribine
publisher SAGE Publishing
series Journal of Central Nervous System Disease
issn 1179-5735
publishDate 2012-04-01
description Multiple Sclerosis (MS) is a chronic inflammatory, immune-mediated, demyelinating disorder of the central nervous system with a heterogeneous clinical presentation and pathology in which activated lymphocytes play an important role in mediating tissue damage. Until recently, all first line therapies for MS were injectable. Several oral medications have been studied for preventative treatment of MS. Cladribine (2-chlorodeoxyadenosine) is a purine nucleoside analog that has been used for the treatment of several hematologic neoplasms, with a unique lymphcytotoxic mechanism of action. Cladribine has been investigated as treatment of MS for more than 15 years. A recent placebo-controlled, double-blind study of cladribine, CLARITY, showed decreased relapse rates, risk of disability progression and MRI measures of disease activity at 96 weeks. Cladribine's strengths included high efficacy and convenient, biannual oral dosing. However, concerns about safety prevented the FDA from approving cladribine in 2011. Thus, use of cladribine for treatment of relapsing and remitting multiple sclerosis will remain off-label.
url https://doi.org/10.4137/JCNSD.S5128
work_keys_str_mv AT terilschreiner currentandemergingtherapiesforthetreatmentofmultiplesclerosisfocusoncladribine
AT augustomiravalle currentandemergingtherapiesforthetreatmentofmultiplesclerosisfocusoncladribine
_version_ 1724535537347330048