Osmotic delivery comprising an insulinotropic peptide and uses thereof
View Patent ↗A suspension formulation of an insulinotropic peptide (e.g., glucagon-like peptide-1 (GLP-1) or exenatide) is described. The suspension formulation comprises (i) a non-aqueous, single-phase vehicle, comprising one or more polymer and one or more one solvent, wherein the vehicle exhibits viscous fluid characteristics, and (ii) a particle formulation comprising the insulinotropic peptide, wherein the peptide is dispersed in the vehicle. The particle formulation further includes a stabilizing component comprising one or more stabilizers, for example, carbohydrates, antioxidants, amino acids, and buffers. Devices for delivering the suspension formulations and methods of use are also described.
1. An osmotic delivery device, comprising,
a reservoir having a first and second ends;
a piston within the reservoir, wherein the piston separates an osmotic engine compartment from a drug reservoir compartment;
the osmotic engine compartment containing an osmotic agent formulation;
the drug reservoir compartment containing a suspension formulation, the suspension formulation comprising,
a particle formulation comprising an insulinotropic peptide, a disaccharide, methionine, and a buffer; and
a non-aqueous, single-phase suspension vehicle that consists essentially of about 20 wt % to about 60 wt % benzyl benzoate and about 80 wt % to about 40 wt % polyvinylpyrrolidone, the suspension vehicle having a viscosity of between about 12,000 to about 18,000 poise at 33° C., wherein the suspension vehicle exhibits viscous fluid characteristics, and the particle formulation is dispersed in the vehicle;
a semipermeable membrane at the first end of the reservoir adjacent the osmotic agent formulation; and
a diffusion moderator at the second end of the reservoir adjacent the suspension formulation.
2. The osmotic delivery device of claim 1 , wherein the insulinotropic peptide is a glucagon-like peptide-1 (GLP-1), a derivative of GLP-1, or an analogue of GLP-1.
3. The osmotic delivery device of claim 2 , wherein the insulinotropic peptide is GLP(7-36)amide.
4. The osmotic delivery device of claim 1 , wherein the insulinotropic peptide is exenatide, a derivative of exenatide, or an analogue of exenatide.
5. The osmotic delivery device of claim 4 , wherein the insulinotropic peptide is exenatide having the amino acid sequence of SEQ ID NO:2.
6. The osmotic delivery device of claim 1 , wherein the buffer is selected from the group consisting of citrate, histidine, succinate, and mixtures therefore.
7. The osmotic delivery device of claim 6 , wherein the buffer is a citrate buffer.
8. The osmotic delivery device of claim 1 , wherein the disaccharide is selected from the group consisting of lactose, sucrose, trehalose, cellobiose, and mixtures thereof.
9. The osmotic delivery device of claim 1 , wherein the particle formulation is a spray dried preparation of particles.
10. The osmotic delivery device of claim 1 , wherein the vehicle is about 50% solvent and about 50% polymer.
11. The osmotic delivery device of claim 1 , wherein the suspension formulation has an overall moisture content of less than or equal to about 10 wt %.
12. A method of treating type II diabetes in a subject in need of such treatment, comprising
delivering the suspension formulation from the osmotic delivery device of claim 1 to the subject at a substantially uniform rate for a period of about one month to about a year.
13. The method of claim 12 , wherein the insulinotropic peptide is GLP-1(7-36)amide and delivering the suspension formulation is at a substantially uniform rate of between about 100 μg/day and about 600 μg/day.
14. The method of claim 12 , wherein the insulinotropic peptide is exenatide and delivering the suspension formulation is at a substantially uniform rate of between about 5 μg/day and about 160 μg/day.
15. A method of manufacturing an osmotic delivery device comprising assembling,
a reservoir having a first and second ends;
a piston within the reservoir, wherein the piston separates an osmotic engine compartment from a drug reservoir compartment;
the osmotic engine compartment containing an osmotic agent formulation;
the drug reservoir compartment containing a suspension formulation, the suspension formulation comprising,
a particle formulation comprising an insulinotropic peptide, a disaccharide, methionine, and a buffer; and
a non-aqueous, single-phase suspension vehicle that consists essentially of about 20 wt % to about 60 wt % benzyl benzoate and about 80 wt % to about 40 wt % polyvinylpyrrolidone, the suspension vehicle having a viscosity of between about 12,000 to about 18,000 poise at 33° C., wherein the suspension vehicle exhibits viscous fluid characteristics, and the particle formulation is dispersed in the vehicle;
a semipermeable membrane at the first end of the reservoir adjacent the osmotic agent formulation; and
a diffusion moderator at the second end of the reservoir adjacent the suspension formulation.