Controlled release compositions of agents that reduce circulating levels of platelets and methods therefor
AssigneeBioVascular, Inc.
InventorsPaul F. Glidden, Alison J. Pilgrim, Stephen R. Hanson
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Abstract
Provided are prophylactic and therapeutic methods of treatment of subjects for the purpose of inhibiting vaso-occlusive events, including embolism, by administering agents, including anagrelide and anagrelide derivatives, which reduce the number of circulating platelets to low normal or to below normal levels. Methods and pharmaceutical preparations comprising such agents are provided.
Claims20
A pharmaceutical composition in unit dosage form comprising:
- (a) a solid support core comprising a plurality of non-pareil sugar spheres at a size range of about 700 microns to about 850 microns (20-25 mesh sieve);
- (b) a substrate layer comprising hydroxypropyl methylcellulose and microparticles of anagrelide hydrochloride monohydrate in hydrated crystal form in an amount that is equivalent to from about 100 μg to about 1000 μg of anagrelide free base, wherein at least 90% of the microparticles are 25 microns or less, and the hydroxypropyl methylcellulose in the substrate layer is present at about 2-4% by weight of the composition;
- (c) a seal coat layer comprising hydroxypropyl methylcellulose, wherein the seal coat layer is present at about at about 2-4% by weight of the composition;
- and
- (d) a release control component comprising ethyl cellulose and hydroxypropyl methyl cellulose at a ratio of about 3:1 and triethyl citrate, wherein the release control component is present at about 1-5% by weight of the composition,
- wherein the seal coat layer is disposed between the substrate layer and the release control component and reduces chemical interaction between the anagrelide hydrochloride monohydrate in the substrate layer and the triethyl citrate in the release control component.
A method of treating essential thrombocythemia in a subject having a circulating platelet count exceeding 600×103 per μl of blood, the method comprising orally administering anagrelide hydrochloride to the subject in a unit dosage at least once daily, wherein the unit dosage form comprises:
- (a) a solid support core comprising a plurality of non-pareil sugar spheres at a size range of about 700 microns to about 850 microns (20-25 mesh sieve);
- (b) a substrate layer comprising hydroxypropyl methylcellulose and microparticles of anagrelide hydrochloride monohydrate in hydrated crystal form in an amount that is equivalent to about 500 μg of anagrelide free base, wherein at least 90% of the microparticles are 25 microns or less, and the hydroxypropyl methylcellulose in the substrate layer is present at about 2-4% by weight of the composition;
- (c) a seal coat layer comprising hydroxypropyl methylcellulose, wherein the seal coat layer is present at about at about 2-4% by weight of the composition;
- and
- (d) a release control component comprising ethyl cellulose and hydroxypropyl methyl cellulose at a ratio of about 3:1 and triethyl citrate, wherein the release control component is present at about 1-5% by weight of the composition;
- wherein the seal coat layer is disposed between the substrate layer and the release control component and reduces chemical interaction between the anagrelide hydrochloride monohydrate in the substrate layer and the triethyl citrate in the release control component.
Dependencies are inferred from the claim text.