Human growth hormone patch formulations

1. A transdermal patch formulation comprising: hGH, wherein the hGH is present in an amount sufficient to achieve a formulation concentration of about 20 mg/ml to 255 mg/ml, sucrose, glycine, and phosphate buffer, wherein the phosphate buffer maintains the pH of the formulation in the range of about 6 to about 8, wherein the hGH, sucrose, and glycine are present in a concentration ratio (mg/ml) of about 0.85:0.80:0.26 to about 0.85:1.20:0.40, and wherein after six months of storage at a temperature of about 4° C. of a transdermal patch comprising the transdermal patch formulation in a dried form, the patch has deamidated, oxidated, cleaved and/or truncated hGH proteins in an amount of about 0.5% to about 13% of hGH and aggregate hGH proteins in an amount of about 0.01% to about 6% of hGH.

2. The transdermal patch formulation according to claim 1 , wherein sucrose is present in an amount sufficient to achieve a formulation concentration of about 11 mg/ml to 300 mg/ml.

3. The transdermal patch formulation according to claim 1 , wherein glycine is present in the formulation in an amount sufficient to achieve a formulation concentration of about 3 mg/ml to about 99 mg/ml.

4. The transdermal patch formulation according to claim 1 , wherein the hGH concentration of the formulation is from about 20 mg/ml to about 170 mg/ml, sucrose is present in an amount sufficient to achieve a formulation concentration of about 22 mg/ml to about 200 mg/ml, glycine is present in the formulation in an amount sufficient to achieve a formulation concentration of about 6 mg/ml to about 66 mg/ml, and phosphate buffer.

5. A transdermal patch formulation of hGH prepared according to a method comprising:

dissolving sucrose and glycine in phosphate buffer to form an excipient solution;

dissolving hGH in the excipient solution to obtain a hGH formulation having a hGH concentration of about 20 mg/ml to 255 mg/ml;

providing the hGH, sucrose and glycine in the formulation at a concentration ratio (mg/ml) of about 0.85:0.80:0.26 to about 0.85:1.20:0.40; and

storing the hGH formulation,

wherein the formulation has a pH of about 6 to 8.

6. The transdermal patch formulation according to claim 5 , wherein the method further comprises removing any non-dissolved particles of hGH after storing the hGH formulation.

7. The transdermal patch formulation according to claim 5 wherein the excipient solution is formed by dissolving sucrose and glycine in a 30 mM phosphate buffer to achieve a formulation concentration of about 100 mg/ml of sucrose and about 33 mg/ml of glycine and a final formulation pH of about 7.5+−0.5; the hGH is dissolved in the excipient solution to achieve a hGH final concentration of about 85 mg/ml to 100 mg/ml; and, after storing the hGH formulation, optionally removing any non-dissolved particles of hGH.

8. A transdermal patch comprising a formulation of hGH, wherein the hGH is present in an amount sufficient to achieve a formulation concentration of about 20 mg/ml to 255 mg/ml, sucrose glycine, and phosphate buffer in an amount sufficient to maintain the formulation pH in the range of about 6 to about 8, wherein after six months of storage at a temperature of about 4° C., the patch has deamidated, oxidated, cleaved and/or truncated hGH proteins in an amount of about 0.5% to about 13% of hGH and aggregate hGH proteins in an amount of about 0.01% to about 6% of hGH, and wherein said hGH, sucrose, and glycine are present in a concentration ratio (mg/ml) of about 0.85:0.80:0.26 to about 0.85:1.20:0.40.

9. The transdermal patch according to claim 8 , wherein after storage for six months at a temperature of about 4° C., the transdermal patch has deamidated, oxidated, cleaved and/or truncated hGH proteins in an amount of about 2% to 10% of hGH.

10. The transdermal patch according to claim 8 , wherein after storage for six months at a temperature of about 4° C., the transdermal patch has aggregate hGH proteins in an amount of about 0.2% to 4% of hGH.