| CPC A61K 38/1793 (2013.01) [A61K 9/0019 (2013.01); A61K 9/08 (2013.01); A61K 39/39591 (2013.01); A61K 47/02 (2013.01); A61K 47/183 (2013.01); A61K 47/26 (2013.01); A61K 47/68 (2017.08); A61P 17/06 (2018.01); A61P 19/02 (2018.01); A61P 29/00 (2018.01); C07K 14/7151 (2013.01); C07K 19/00 (2013.01); C07K 2319/30 (2013.01); C07K 2319/32 (2013.01)] | 48 Claims |
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1. A method of treating a patient having rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, or psoriasis, comprising administering to said patient a pharmaceutical composition comprising between 75 mM and 150 mM NaCl, between 5 mM and 100 mM arginine, between 0.5% and 2% (w/v) sucrose, and between 40 mg/mL and 100 mg/mL etanercept, wherein the pharmaceutical composition comprises less than 2.0 mM total additional buffering agent, and the pH of the pharmaceutical composition is between 6.1 and 6.5.
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