New Data Suggest Oral Laquinimod May Confer Neuroprotection in Addition to Immunomodulation in the Treatment of Multiple Sclerosis

Stuart SchlossmanMS Drug Therapies, Multiple Sclerosis, Oral MS Medications

Press Release Source: Active Biotech On Thursday April 15, 2010, 12:50 pm

LUND, SWEDEN–(Marketwire – 04/15/10) –

– Enhanced levels of brain derived neurotrophic factor, possibly contributing to neuroprotection, were shown in laquinimod treated multiple sclerosis (MS) patients

– Laquinimod significantly reduce demyelination and axonal damage as shown in animal models

– Two ongoing pivotal, global phase III clinical trials are fully enrolled and results are anticipated next year

Jerusalem, Israel and Lund, Sweden, April 15, 2010 – Teva Pharmaceutical Industries Ltd. and Active Biotech (NASDAQ OMX NORDIC: ACTI) today announced results from several studies demonstrating that laquinimod, a novel, investigational once-daily oral immunomodulator for relapsing remitting multiple sclerosis (RRMS) may have neuroprotective properties in addition to its anti-inflammatory effects. These studies were presented at the 62(nd) Annual Meeting of the American Academy of Neurology (AAN).

New data from studies in RRMS patients demonstrate that treatment with laquinimod results in a significant increase in brain derived neurotrophic factor, a key protein responsible for the maintenance of mature neurons.

Additionally, data from new animal models show that following treatment with laquinimod there were significant reduction in the extent of demyelination, and more axonal preservation within spinal cord lesions. Furthermore, treatment with laquinimod inhibited the infiltration of inflammatory cells, into the spinal cord and brain as well as causing a positive shift in specific white blood cells involved in MS pathology.

These findings suggest laquinimod may have neuroprotective properties in addition to anti-inflammatory effects. Coupled with the Phase IIb study results, which demonstrated oral laquinimod to be effective and safe in RRMS patients, these data provide further insight into the contributing factors surrounding the favorable benefit-risk profile associated with this compound to date.

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