Pharmaceutical methods, dosing regimes and dosage forms for...

A - Human Necessities – 61 – K

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A61K 9/48 (2006.01) A61K 31/19 (2006.01)

Patent

CA 2532207

In general, the invention relates to a pharmaceutical dose having R- flurbiprofen as the active ingredient that upon oral administration of a single dose to a fasting subject provides a Cmax of about 30-95 ~g per mL. When the dose is administered to an individual having mild-to-moderate Alzheimer's disease (or desiring protection against Alzheimer's disease) twice daily for at least 4 months according to the described guidelines, an improvement or lessening in decline of cognitive function as characterized by cognition tests is observed in the patient. The composition of the invention is formulated with one or more pharmaceutically acceptable excipients, salts or carriers.

La présente invention se rapporte à une dose pharmaceutique renfermant du R-flurbiprofène à titre d'ingrédient actif, la valeur C¿max? lors de l'administration par voie orale d'une dose unique à un sujet à jeun étant comprise entre environ 30 et 95 µg par ml. Lorsque la dose est administrée à un individu atteint de la maladie d'Alzheimer à un degré léger à moyen (ou à un individu désirant être protégé contre la maladie d'Alzheimer), et ce deux fois par jour pendant au moins quatre mois selon les directives décrites, on observe chez le malade une amélioration des fonctions cognitives, ou une atténuation de la détérioration des fonctions cognitives, telles que caractérisées par des tests cognitifs. La composition selon l'invention est formulée avec un ou plusieurs excipients, sels ou véhicules pharmaceutiquement acceptables.

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