Safinamide: from molecular targets to a new anti-Parkinson drug
by
Caccia C, Maj R, Calabresi M, Maestroni S,
Faravelli L, Curatolo L, Salvati P, Fariello RG.
Newron Pharmaceuticals Spa, Bresso, MI, Italy.
carla.caccia@newron.com
Neurology. 2006 Oct 10;67(7 Suppl 2):S18-23.

ABSTRACT

Ideal treatment in Parkinson's disease (PD) aims at relieving symptoms and slowing disease progression. Of all remedies, levodopa remains the most effective for symptomatic relief, but the medical need for neuroprotectant drugs is still unfulfilled. Safinamide, currently in phase III clinical trials for the treatment of PD, is a unique molecule with multiple mechanisms of action and a very high therapeutic index. It combines potent, selective, and reversible inhibition of MAO-B with blockade of voltage-dependent Na+ and Ca2+ channels and inhibition of glutamate release. Safinamide has neuroprotective and neurorescuing effects in MPTP-treated mice, in the rat kainic acid, and in the gerbil ischemia model. Safinamide potentiates levodopa-mediated increase of DA levels in DA-depleted mice and reverses the waning motor response after prolonged levodopa treatment in 6-OHDA-lesioned rats. Safinamide has excellent bioavailability, linear kinetics, and is suitable for once-a-day administration. Therefore, safinamide may be used in PD to reduce l-dopa dosage and also represents a valuable therapeutic drug to test disease-modifying potential.

Safinamide
Phenelzine
Befloxatone
Brofaromine
Moclobemide
Isocarboxazid
Tranylcypromine
Atypical depression
Drugs for depression
MAO, emotion and stress
Parkinson's disease: resources

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