Stable pharmaceutical composition containing factor VIII
View Patent ↗The invention relates to a stable solid pharmaceutical composition comprising factor VIII. Such a composition is devoid of amino acids and comprises: (a) factor VIII; (b) a surfactant; (c) calcium chloride; (d) sucrose; (e) sodium chloride; (f) trisodium citrate; and (g) a buffer devoid of amino acids; and has a pH from 6 to 8 prior to lyophilization and after reconstitution in water for injection. The invention also relates to the liquid pharmaceutical composition obtainable after dilution of said stable solid pharmaceutical composition with sterile water optionally containing sodium chloride.
1. A solid pharmaceutical composition comprising a lyophilized solution devoid of amino acids, wherein said solution comprises:
(a) mature recombinant porcine factor VIII, wherein said mature recombinant porcine factor VIII extends from amino acid residue 20 to amino acid residue 1467 of;
(b) a surfactant;
(c) calcium chloride;
(d) sucrose;
(e) sodium chloride;
(f) trisodium citrate; and
(g) a buffer devoid of amino acids;
wherein said solution has a pH from 6 to 8 prior to lyophilization and wherein said solid pharmaceutical composition results in a solution having a pH from 6 to 8 after reconstitution in water for injection.
2. The solid pharmaceutical composition of claim 1 wherein the surfactant is polysorbate.
3. The solid pharmaceutical composition of claim 2 wherein the surfactant is a polysorbate 80.
4. The solid pharmaceutical composition of claim 1 wherein the buffer devoid of amino acids is TRIS(hydroxymethyl)methylamine.
5. The solid pharmaceutical composition of claim 1 wherein the solution devoid of amino acids has a pH from 6.5 to 7.5 prior to lyophilization and wherein said solid pharmaceutical composition results in a solution having a pH from 6.5 to 7.5 after reconstitution in water for injection.
6. The solid pharmaceutical composition of claim 1 , wherein the solution devoid of amino acids comprises:
(a) a concentration of factor VIII from 50 to 10,000 porcine units/ml for mature recombinant porcine factor VIII;
(b) a concentration of surfactant from above critical micellar concentration to 1% v/v;
(c) a concentration of calcium chloride from 0.5 to 10 mM;
(d) a concentration of sucrose from 5 to 50 mM;
(e) a concentration of sodium chloride from 0.15 to 0.5 M;
(f) a concentration of trisodium citrate from 1 to 50 mM; and
(g) a concentration of a buffer devoid of amino acids from 1 to 50 mM.
7. The liquid pharmaceutical composition obtainable after dilution of a solid pharmaceutical composition of claim 1 with sterile water optionally containing sodium chloride.