US2012214749A1PendingUtilityA1
Microparticles comprising somatostatin analogues
Est. expiryNov 14, 2023(expired)· nominal 20-yr term from priority
A61P 35/04A61P 5/50A61P 37/06A61P 9/10A61P 9/00A61P 3/04A61P 5/02A61P 35/02A61P 3/10A61P 35/00A61P 27/02A61P 29/00A61P 3/00A61P 25/00A61P 1/12A61P 19/02A61P 1/04A61P 17/06A61P 1/18A61P 13/12A61K 38/31A61K 9/1647Y10S977/788A61K 9/16A61K 9/14
47
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Claims
Abstract
Disclosed are microparticles comprising a somatostatin analogue embedded in a biocompatible pharmacologically acceptable polymer matrix for a long acting release and pharmaceutical compositions comprising such microparticles.
Claims
exact text as granted — not AI-modified1 . A method of treating a disease or disorder with an aetiology comprising or associated with excess GH- and/or IGF-1 secretion in a subject in need thereof which comprises administering microparticles where said microparticles comprising cyclo[{4-(NH 2 —C 2 H 4 —NH—CO—O—)Pro}-Phg-DTrp-Lys-Tyr(4-Bzl)-Phe] in free form, salt form or protected form embedded in a polymer matrix wherein the polymer matrix comprises a linear and a star polylactide-co-glycolide.
2 . A method according to claim 1 wherein the cyclo[{4-(NH 2 —C 2 H 4 —NH—CO—O—) Pro}-Phg-DTrp-Lys-Tyr(4-Bzl)-Phe] is in pamoate salt form.
3 . A method according to claim 1 wherein the polymer matrix comprises a linear polylactide-co-glycolide polymer and a star polylactide-co-glycolide polymer having a weight average molecular weight of about 50,000 Da.
4 . A method according to claim 1 wherein the ratio of linear to star polylactide-co-glycolide is 50:50.
5 . A method according to claim 1 wherein the cyclo[{4-(NH 2 —C 2 H 4 —NH—CO—O—) Pro}-Phg-DTrp-Lys-Tyr(4-Bzl)-Phe] is an amorphous powder having a particle size less than about 5 microns.
6 . A method according to claim 1 where said microparticles further comprising a surfactant, a porosity influencing agent and/or a basic salt.
7 . A method of treating a disease or disorder with an aetiology comprising or associated with excess GH- and/or IGF-1 secretion in a subject in need thereof which comprises administering a composition comprising microparticles where said microparticles comprising cyclo[{4-(NH 2 —C 2 H 4 —NH—CO—O—)Pro}-Phg-DTrp-Lys-Tyr(4-Bzl)-Phe] in free form, salt form or protected form embedded in a polymer matrix wherein the polymer matrix comprises a linear and a star polylactide-co-glycolide. and a water-based vehicle comprising a wetting agent.
8 . A method according to claim 7 wherein the wetting agent comprises a poloxamer and/or a polyoxyethylene-sorbitan-fatty acid ester.
9 . A method according to claim 7 wherein the vehicle comprises a tonicity agent.
10 . A method according to claim 7 wherein the vehicle comprises a viscosity increasing agent.Cited by (0)
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