CPC A61K 47/26 (2013.01) [A61K 9/08 (2013.01); A61K 31/7004 (2013.01); A61K 31/728 (2013.01); A61K 33/06 (2013.01); A61K 33/14 (2013.01); A61K 35/28 (2013.01); A61K 35/30 (2013.01); A61K 47/02 (2013.01); A61K 47/12 (2013.01); A61K 47/36 (2013.01); A61P 27/02 (2018.01)] | 29 Claims |
1. A method for treating a retinal disease, the method comprising
administering, to the eye of a human subject having a retinal disease, an effective amount of a pharmaceutical composition comprising
(a) a population of cells, and
(b) a solution comprising
(i) about 0.1-1.2 mM CaCl2, about 0.05-5 mM MgCl2, about 1-2.5 mM KCl, about 0.5-2 mM sodium citrate, about 15-17 mM dextrose, and about 125-175 mM NaCl, or
(ii) about 0.5-0.9 mM CaCl2, about 0.2-0.4 mM MgCl2, about 1.6-2.4 mM KCl, about 0.8-1.2 mM sodium citrate, about 13-19 mM dextrose, and about 116-174 mM NaCl, or
(iii) about 0.008-0.012% CaCl2 dihydrate, about 0.0048-0.0072% MgCl2 hexahydrate, about 0.012-0.018% KCl, about 0.028-0.042% sodium citrate dihydrate, about 0.23-0.35% dextrose, and about 0.68-1.02% NaCl.
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