Compositions, devices and methods of use thereof for the treatment of cancers
The use of GLP-1 receptor agonists, such as glucagon-like peptide-1 (GLP-1) or exenatide, for the treatment of cancer is described. The GLP-1 receptor agonists are typically delivered using an implanted osmotic delivery device that provides for continuous delivery of the GLP-1 receptor agonist for at least one month. Additional beneficial agents, such as anticancer agents, can also be administered.
1. An implantable osmotic delivery device comprising a suspension formulation, the suspension formulation comprising: (a) a particle formulation comprising semaglutide, sucrose and methionine, the particle formulation having a ratio of semaglutide:(sucrose+methionine) of from about 2:1 to about 20:1, and (b) a non-aqueous vehicle formulation, wherein the particle formulation is dispersed in the non-aqueous vehicle formulation.
2. The implantable osmotic delivery device of claim 1 , wherein the particle formulation additionally comprises: a buffer selected from the group consisting of citrate, histidine, succinate, and mixtures thereof; the particle formulation is a spray dried preparation of particles, and the suspension formulation has an overall moisture content of less than or equal to about 10 wt %.
3. The implantable osmotic delivery device of claim 1 , wherein (a) the particle formulation additionally comprises a buffer and (b) the vehicle formulation is a single-phase suspension vehicle comprising one or more pyrrolidone polymers and one or more solvents selected from the group consisting of lauryl lactate, lauryl alcohol, benzyl benzoate, and mixtures thereof.
4. The implantable osmotic delivery device of claim 3 , wherein the buffer is selected from the group consisting of citrate, histidine, succinate, and mixtures thereof.
5. The implantable osmotic delivery device of claim 1 , wherein the particle formulation is a spray dried preparation of particles.
6. The implantable osmotic delivery device of claim 1 , wherein the vehicle consists essentially of polyvinylpyrrolidone and benzyl benzoate.
7. The implantable osmotic delivery device of claim 1 , wherein the vehicle is about 50% solvent and about 50% polymer.
8. The implantable osmotic delivery device of claim 1 , wherein the suspension formulation has an overall moisture content of less than or equal to about 10 wt %.