Anti-botulism antibody coformulations
View Patent ↗This invention relates to stable formulations of multiple antibodies comprising a plurality of anti-botulism antibodies and an effective amount of a succinate buffer, an effective amount of arginine, wherein the antibodies are present in substantially equal concentrations and the pH of the formulation is between about 5 and about 6.5.
1. A stable pharmaceutical formulation comprising a plurality of antibodies directed to at least one serotype of botulinum neurotoxin (BoNT) each of which antibodies specifically recognizes and binds a different epitope or a different BoNT serotype and is present at a concentration of at least about 1 mg/mL, an effective amount of a succinate buffer in a concentration from about 5 mM to about 15 mM, and an effective amount of arginine in a concentration of from about 140 mM to about 144 mM, wherein the pH of the formulation is between about 5 and about 6.5, wherein the formulation is stable at room temperature for at least 30 days, and wherein the plurality of antibodies comprises a first antibody comprising a heavy chain variable region of SEQ ID NO.3 and a light chain variable region of SEQ ID NO.4, a second antibody comprising a heavy chain variable region of SEQ ID NO.1 and a light chain variable region of SEQ ID NO.2, and a third antibody comprising a heavy chain variable region of SEQ ID NO.5 and a light chain variable region of SEQ ID NO.6.
2. The formulation of claim 1 , wherein each antibody is present at a concentration between about 1 mg/mL and about 5 mg/mL.
3. The formulation of claim 1 , wherein the pH is at about 6.
4. The formulation of claim 1 , wherein the pH is at about 6.5.
5. The formulation of claim 1 , wherein the succinate buffer comprises sodium succinate.
6. The formulation of claim 1 , wherein the arginine is present in a concentration of about 142 mM.
7. The formulation of claim 1 , further comprising a surfactant.
8. The formulation of claim 7 , wherein the surfactant comprises at least one selected from the group consisting of polyoxyethylensorbitan fatty acid ester, polyoxyethylene alkyl ether, alkylphenylpolyoxyethylene ether, polyoxyethylene polyoxypropylene copolymer, and sodium dodecyl sulphate.
9. The formulation of claim 8 , wherein the surfactant is polyoxyethylensorbitan fatty acid ester.
10. The formulation of claim 9 , wherein the polyoxyethylensorbitan fatty acid ester is polysorbate 20 or polysorbate 80.
11. The formulation of claim 9 , wherein the polyoxyethylensorbitan fatty acid ester is polysorbate 80.
12. The formulation of claim 7 , wherein the surfactant is present in a concentration of from about 0.002% (w/v) to about 0.1% (w/v).
13. The formulation of claim 7 , wherein the surfactant is present in a concentration of from about 0.003% (w/v) to about 0.007% (w/v).
14. The formulation of claim 1 , further comprising a stabilizer and/or a cryoprotectant and/or a lyoprotectant.
15. The formulation of claim 14 , wherein the stabilizer comprises at least one selected from the group consisting of a sugar, an amino acid, a polyol, a surfactant, an antioxidant, a preservative, a cyclodextrine, a polyethyleneglycol, albumin and a salt.
16. The formulation of claim 1 , wherein the formulation is stable at a temperature from about 2.0° C. to about 8.0° C. for at least about five years.
17. The formulation of claim 1 , wherein the formulation is stable at a temperature from about −80° C. to about −20° C. for at least about two years.
18. The formulation of claim 1 , wherein the formulation is physically stable.
19. The formulation of claim 1 , wherein the formulation is chemically stable.
20. The formulation of claim 1 , wherein the formulation is biologically stable.
21. A lyophilized formulation prepared by lyophilizing the formulation of claim 1 .