IP Library Granted Patent US 9,254,307
Granted Patent B2
US 9,254,307 · App. 12/784,343 · Granted Feb 9, 2016

Polymeric delivery formulations of leuprolide with improved efficacy

Inventors: Richard L. Dunn (Fort Collins, CO); John Steven Garrett (Fort Collins, CO); Harish Ravivarapu (Union City, CA); Bhagya L. Chandrashekar (Fort Collins, CO)
Assignee: Tolmar Therapeutics, Inc.
A61K38/09A61K9/0024A61K9/19A61K47/22A61K47/34B65D81/3205
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Quick Facts
Patent No.
US 9,254,307
App. No.
12/784,343
Granted
Feb 9, 2016
Kind
B2
Abstract

The present invention is directed to a flowable composition that is suitable for use as a controlled release implant. The flowable composition includes a biodegradable thermoplastic polyester that is at least substantially insoluble in aqueous medium or body fluid. The flowable composition also includes a biocompatible polar aprotic solvent. The biocompatible polar aprotic solvent is miscible to dispersible in aqueous medium or body fluid. The flowable composition also includes leuprolide acetate.

Claims (4)

1. A flowable composition suitable for use to form an in situ, single body controlled release implant, the composition consisting essentially of a non-aqueous, liquid solution of: (a) a biodegradable thermoplastic copolymer of lactide and glycolide that has a carboxy terminal group, that is at least substantially insoluble in aqueous medium or body fluid, and that has a weight average molecular weight of 15,000 to 45,000; (b) N-methyl-2-pyrrolidone; and (c) leuprolide acetate, wherein the copolymer is present in the composition at 30 wt % to 50 wt %; the N-methyl-2- pyrrolidone is present in the composition at 50 wt % to 70 wt % and the leuprolide acetate is present in the composition at 2 wt % to 8 wt %; and the composition is formulated for administration to a male patient about once per month to produce in situ the single body implant thereby reducing serum testosterone levels in the male patient.

2. A biodegradable implant formed in situ, in a male patient, by the steps comprising: (a) injecting 0.2 to 0.5 ml of the flowable composition of claim 1 within the body of the patient; and (b) allowing the N-methyl-2-pyrrolidone to dissipate to produce a solid, monolithic biodegradable implant of a microporous matrix of a core surrounded by a skin.

3. A method of reducing serum testosterone levels in a male human comprising injecting subcutaneously into the male human 0.2 ml to 0.5 ml of a flowable composition consisting essentially of a non-aqueous, liquid solution of: (a) a biodegradable thermoplastic copolymer of lactide and glycolide that has a carboxy terminal group, that is at least substantially insoluble in aqueous medium or body fluid, and that has a weight average molecular weight of 15,000 to 45,000; (b) N-methyl-2-pyrrolidone; and (c) leuprolide acetate in an amount sufficient to reduce LHRH levels in a human; wherein the copolymer is present in the composition at 30 wt % to 50 wt %; the N-methyl-2-pyrrolidone is present in the composition at 50 wt % to 70 wt % and the leuprolide acetate is present in the composition at 2 wt % to 8 wt %;

whereupon the flowable composition forms in situ a monolithic solid implant of a microporous matrix of a core surrounded by a skin within a body tissue of the male human by diffusion of the N-methyl-2-pyrrolidone into the body fluid of the male human and precipitation of the copolymer of lactide and glycolide.

Assignments (2)
SECURITY INTEREST Recorded Oct 2, 2017
From: TOLMAR THERAPEUTICS, INC.; TOLMAR, INC.
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT
Reel/Frame 043756/0502 →
CHANGE OF NAME Recorded Jun 7, 2012
From: QLT USA, INC.
To: TOLMAR THERAPEUTICS, INC.
Reel/Frame 028339/0496 →
Continuity (8)
Continuation 11643505 · Dec 21, 2006
Continuation 10872671 · Jun 21, 2004
Continuation 10373400 · Feb 24, 2003
Continuation 09711758 · Nov 13, 2000
Continuation In Part 09666174 · Sep 21, 2000
Continuation In Part 09643289 · Aug 22, 2000
Continuation 09181355 · Oct 28, 1998
Related Publication 20100234305A1 · Sep 16, 2010