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Injectable subcutaneous formulation comprising risperidone capable of forming a solid, microporous implant in a patient
专利权人:
TOLMAR THERAPEUTICS; INC.
发明人:
DADEY, ERIC
申请号:
NZ58186208
公开号:
NZ581862A
申请日:
2008.02.13
申请国别(地区):
NZ
年份:
2012
代理人:
摘要:
Disclosed is a flowable composition which comprises: (a) a biodegradable thermoplastic polymer that is at least substantially insoluble in body fluid (such as a poly(DL-lactide-co-glycolide)), and wherein said biodegradable thermoplastic polymer is a polyester of one or more hydroxycarboxylic acids, or is a polyester of a combination of one or more diols and one or more dicarboxylic acids; (b) a biocompatible polar aprotic organic liquid that is highly water soluble and which comprises an amide, an ester, a carbonate, a ketone, an ether, a sulfonyl, or any combination thereof (and which is preferably selected from N-methyl-2-pyrrolidone, 2-pyrrolidone, N,N-dimethylformamide, dimethyl sulfoxide, caprolactam, or combinations thereof); and (c) risperidone, 9-hydroxyrisperidone or a pharmaceutically acceptable organic or inorganic salt thereof; and wherein the flowable composition is an injectable subcutaneous formulation capable of forming a solid, microporous implant in a patient by diffusion of the biocompatible polar aprotic organic liquid out of the flowable composition into the body fluid, so that the flowable composition coagulates to form the implant.
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