Slow release pharmaceutical composition made of microparticles
Abstract
Pharmaceutical composition made of microparticles for the slow release of an active substance at least during a period covering the 6th month after injection of said composition, said composition comprising a group of microparticles made of a copolymer of the PLGA type which incorporate an active substance in the form of a water insoluble peptide salt; said copolymer furthermore comprising at least 75% of lactic acid and an inherent viscosity between 0.1 and 0.9 dl/g, as measured in chloroform at 25° C. and at a polymer concentration of 0.5 g/dL; said microparticles furthermore having a size distribution defined as follows:—D (v,0.1) is between 10 and 30 micrometers,—D (v,0.5) is between 30 and 70 micrometers,—D(v,0.9) is between 50 and 110 micrometers.
Claims
exact text as granted — not AI-modified1 - 15 . (canceled)
16 . A pharmaceutical composition comprising microparticles comprising 22.5 mg triptorelin in the form of triptorelin pamoate, wherein the microparticles are made of poly(D,L lactide-co-glycolide) (PLGA), wherein the PLGA comprises at least 75% lactide, and wherein the triptorelin pamoate is released from the pharmaceutical composition in an immediate amount within hours following injection into a patient and then constantly released over a period of at least 168 days, wherein the composition comprises two groups of microparticles, wherein the two groups of microparticles are a first group of microgranules and a second group of microgranules.
17 . The pharmaceutical composition of claim 16 , wherein the first group of microgranules and the second group of microgranules are mixed to have a 50:50 dose ratio of triptorelin.
18 . The pharmaceutical composition of claim 16 , wherein the pharmaceutical composition is administered to the patient once about every six months.
19 . The pharmaceutical composition of claim 16 , wherein the PLGA in the first group of microgranules comprises at least 85% lactide.Cited by (0)
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