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AssigneeEuro-Celtique S.A.
InventorsJoanne Heafield, Trevor John Knott, Stewart Thomas Leslie, Sandra Therese Antoinette Malkowska, Ronald Brown Miller, Derek Allan Prater, Kevin John Smith
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Sustained release pharmaceutical formulations containing morphine, or a pharmaceutically acceptable salt thereof, as active ingredient, suitable for administration on a once daily basis, are disclosed. In a first aspect, an orally administrable sustained release unit dosage form gives a peak plasma level at 1.0 to 6 hours after administration. In a second aspect, the formulation provides a W.sub.50 for the M-6-G metabolite for morphine of between 4 and 12 hours. A third aspect concerns the pharmaceutical unit dosage form obtained by compressing multiparticulates comprising a pharmaceutically active substance in a matrix of hydrophobic fusible material having a melting point of from 35 to 150.degree. C.
An oral sustained release pharmaceutical formulation comprising multiparticulates including morphine or a pharmaceutically acceptable salt thereof dispersed in a matrix of a natural or synthetic wax or oil with a melting point of from about 35 degrees C. to about 100 degrees C., such that the multiparticulates provide a time to peak plasma level of morphine in about 1.0 to about 6.0 hours after administration, and when administered in an effective amount, provide morphine plasma levels which are effective for 24 hourly dosing, characterized by a width of the plasma profile at 50% Cmax (W.sub.50) for the morphine-6-glucoronide metabolite of morphine of between 4 and 12 hours, said multparticulates being prepared by mixing together said morphine or salt thereof and said natural or synthetic wax or oil at a rate and energy input sufficient to cause said natural or synthetic wax or oil to melt or soften whereby it forms said multiparticulates containing said morphine or salt thereof.
An oral sustained release pharmaceutical formulation comprising multiparticulates including morphine or a pharmaceutically acceptable salt thereof dispersed in a matrix of a natural or synthetic wax or oil with a melting point of from about 35 degrees C. to about 100 degrees C., said multparticulates having in vitro release characteristics such that the multiparticulates, when assessed by the modified European Pharmacopeia Basket Method at 100 rpm in 900 ml aqueous buffer at pH 6.5 containing 0.5% polysorbate at 37 degrees C., releases from 5 to 30% of morphine two hours after start of test, 15 to 50% at 4 hours after start of test;
An oral sustained release pharmaceutical formulation comprising multiparticulates including morphine or a pharmaceutically acceptable salt thereof and a natural or synthetic wax or oil, said multiparticulates characterized by a width of the plasma profile at 50% Cmax (W.sub.50) for said morphine of between 4 and 12 hours after administration and when administered in an effective amount, provide sufficient analgesia for about 24 hours after administration.
Dependencies are inferred from the claim text.