FORMULATIONS OF GUANYLATE CYCLSE C AGONISTS AND METHODS OF USE
The invention provides low-dose formulations of guanylate cyclase-C (“GCC”) agonist peptides and methods for their use. The formulations of the invention can be administered either alone or in combination with one or more additional therapeutic agents, preferably an inhibitor of cGMP-dependent phosphodiesterase or a laxative.
1 - 18 . (canceled)
19 . An oral dosage formulation comprising at least one guanylate cyclase-C(GCC) agonist peptide and at least one pharmaceutically acceptable excipient,
wherein the amount of the GCC agonist peptide per unit dose is 0.01 mg to 10 mg,
wherein the GCC agonist peptide has the amino acid sequence of any one of SEQ ID NO: 9 and 56-249, and
wherein the GCC agonist peptide has a chromatographic purity of no less than 91%.
20 . The oral dosage formulation of claim 19 , wherein the GCC agonist peptide has a chromatographic purity of no less than 95%.
21 . The oral dosage formulation of claim 19 , wherein the GCC agonist peptide has a total impurity content of no greater than 9%.
22 . The oral dosage formulation of claim 19 , wherein the oral dosage formulation is substantially free of inorganic acids and carboxylic acids.
23 . The oral dosage formulation of claim 19 , wherein the GCC agonist peptide is SEQ ID NO: 56 or SEQ ID NO: 9.
24 . The oral dosage formulation of claim 19 , wherein the amount of GCC agonist peptide per unit dose is selected from the group consisting of 0.1 mg, 0.3 mg, 1.0 mg, 3.0 mg, 6.0 mg, 9.0 mg, and 9.5 mg.
25 . The oral dosage formulation of claim 19 , wherein the oral dosage formulation is a solid formulation and wherein the unit dose is a powder, granule, sachet, troche, tablet, or capsule.
26 . The oral dosage formulation of claim 19 , wherein the at least one pharmaceutically acceptable excipient comprises an inert carrier.
27 . The oral dosage formulation of claim 26 , wherein the inert carrier is selected from the group consisting of mannitol, lactose, a microcrystalline cellulose, and starch.
28 . The oral dosage formulation of claim 26 , wherein the inert carrier has a particle size of 50 to 900 microns.
29 . The oral dosage formulation of claim 19 , wherein the at least one pharmaceutically acceptable excipient comprises a divalent cation salt.