Sustained releasable parenteral pharmaceutical preparations and method of producing the same
AssigneeTakeda Chemical Industries, Ltd.
InventorsYutaka Yamagata, Katsumi Iga, Hiroaki Okada
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AssigneeTakeda Chemical Industries, Ltd.
InventorsYutaka Yamagata, Katsumi Iga, Hiroaki Okada
Estimating the term…
A parenteral pharmaceutical preparation comprises a matrix containing a physiologically active peptide or protein and a polyglycerol diester of a saturated fatty acid, and the matrix is in a solid form at room temperature. The molecular weight of the physiologically active peptide or protein is 2,000 dalton or more. The saturated fatty acid includes fatty acids having about 16 to 30 carbon atoms such as palmitic acid, stearic acid, etc. The matrix may be in a pillar or granular form. The parenteral pharmaceutical preparation can be used as an injectable solid administered subcutaneously or intramuscularly (for example, a pellet or tablet for implantation), a suppository or the like, and can release the physiologically active peptide or protein sustainedly for a prolonged period of one week or more.
A sustained releasable parenteral pharmaceutical preparation in cylindrical or columnar form which comprises a matrix containing an interferon-.alpha. and a polyglycerol diester of stearic acid or palmitic acid, wherein said polyglycerol has an average polymerization degree of 4.
A method of producing a sustained releasable parenteral pharmaceutical preparation, which method comprises mixing an interferon-.alpha. with a molten or softened polyglycerol diester of stearic acid or palmitic acid and molding the molten mixture into a cylindrical or columnar form, wherein said polyglycerol has an average polymerization degree of 4.
Dependencies are inferred from the claim text.