Literature DB >> 19527103

Oral laquinimod therapy in relapsing multiple sclerosis.

Jana Preiningerova1.   

Abstract

BACKGROUND: Multiple sclerosis (MS) is a chronic autoimmune disease of the CNS. Early treatment reduces the number of relapses, limits progression of disability, and improves quality of life; however, existing therapies are only partially effective and require parenteral administration.
OBJECTIVE: To review current experience with laquinimod as a novel immunomodulatory therapy for MS.
RESULTS: Laquinimod is a new quinolonecarboxamide that has demonstrated efficacy in animal models of several autoimmune diseases, including MS. It shows immunomodulatory effects, likely through Th1/Th2 shift, but does not lead to immunosuppression. Laquinimod is metabolized in the liver, primarily by the CYP3A4 enzyme. Phase II studies in relapsing MS demonstrate a dose-response effect on disease activity, measured by number of active lesions on brain magnetic resonance imaging, and show favorable tolerability and safety based on clinical and laboratory indicators. Two Phase III studies currently in progress are evaluating the efficacy of laquinimod 0.6 mg/day in relapsing MS. The drug was granted a fast track review by the FDA in 2009.
CONCLUSION: Laquinimod is a novel, orally administered immunomodulator that has advanced to the pre-submission stage and may become an alternative to the current injectable first-line treatments for relapsing MS.

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Year:  2009        PMID: 19527103     DOI: 10.1517/13543780903044944

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  9 in total

Review 1.  The long and winding road for the development of tasquinimod as an oral second-generation quinoline-3-carboxamide antiangiogenic drug for the treatment of prostate cancer.

Authors:  John T Isaacs
Journal:  Expert Opin Investig Drugs       Date:  2010-10       Impact factor: 6.206

2.  The Aryl Hydrocarbon Receptor (AhR) as a Drug Target for Cancer Chemotherapy.

Authors:  Stephen Safe; Yating Cheng; Un-Ho Jin
Journal:  Curr Opin Toxicol       Date:  2017-02-01

3.  Reduced astrocytic NF-κB activation by laquinimod protects from cuprizone-induced demyelination.

Authors:  Wolfgang Brück; Ramona Pförtner; Trinh Pham; Jingya Zhang; Liat Hayardeny; Victor Piryatinsky; Uwe-Karsten Hanisch; Tommy Regen; Denise van Rossum; Lars Brakelmann; Karin Hagemeier; Tanja Kuhlmann; Christine Stadelmann; Gareth R John; Nadine Kramann; Christiane Wegner
Journal:  Acta Neuropathol       Date:  2012-07-06       Impact factor: 17.088

4.  Multiple sclerosis: pathogenesis and treatment.

Authors:  Ingrid Loma; Rock Heyman
Journal:  Curr Neuropharmacol       Date:  2011-09       Impact factor: 7.363

Review 5.  Development of oral immunomodulatory agents in the management of multiple sclerosis.

Authors:  Richard Nicholas; Paolo Giannetti; Ali Alsanousi; Tim Friede; Paolo A Muraro
Journal:  Drug Des Devel Ther       Date:  2011-05-10       Impact factor: 4.162

6.  Disease-modifying drug initiation patterns in commercially insured multiple sclerosis patients: a retrospective cohort study.

Authors:  Jay M Margolis; Robert Fowler; Barbara H Johnson; Cheryl A Kassed; Kristijan Kahler
Journal:  BMC Neurol       Date:  2011-10-06       Impact factor: 2.474

7.  Effects of low dose methotrexate on relapsing-remitting multiple sclerosis in comparison to Interferon β-1α: A randomized controlled trial.

Authors:  Fereshteh Ashtari; Mohammad Reza Savoj
Journal:  J Res Med Sci       Date:  2011-04       Impact factor: 1.852

8.  Co-Transplantation of Human Neurotrophic Factor Secreting Cells and Adipose-Derived Stem Cells in Rat Model of Multiple Sclerosis.

Authors:  Shahnaz Razavi; Nazem Ghasemi; Mohammad Mardani; Hossein Salehi
Journal:  Cell J       Date:  2017-12-01       Impact factor: 2.479

9.  Laquinimod dampens hyperactive cytokine production in Huntington's disease patient myeloid cells.

Authors:  Lucianne Dobson; Ulrike Träger; Ruth Farmer; Liat Hayardeny; Pippa Loupe; Michael R Hayden; Sarah J Tabrizi
Journal:  J Neurochem       Date:  2016-04-05       Impact factor: 5.372

  9 in total

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