Stable aqueous formulations of adenovirus vectors

1. An aqueous formulation comprising an adenovirus vector containing a whole transgene and carboxymethyl cellulose or a salt form thereof at a concentration ranging from about 0.5 mg/mL to about 10 mg/mL.

2. The formulation of claim 1 , wherein the carboxymethyl cellulose or salt form thereof is sodium carboxymethyl cellulose and wherein the sodium carboxymethyl cellulose has an average molecular weight between about 20000 Da and about 1000000 Da.

3. The formulation of claim 2 , wherein the sodium carboxymethyl cellulose has an average molecular weight of about 90000 Da.

4. The formulation of claim 1 , further comprising at least one displaced buffer having an ionizable group with a pKa value at least one unit higher or lower than the pH of the formulation and having no ionizable group with a pKa value within one unit of the pH of the formulation.

5. The formulation of claim 4 , wherein the displaced buffer is selected from the group consisting of tris(hydroxymethyl)aminomethane (TRIS), benzoate ion, and a combination thereof.

6. The formulation of claim 1 , wherein the pH of the formulation is between 5 and 8.

7. The formulation of claim 1 , further comprising a tonicity modifier selected from the group consisting of 1,2-propanediol, glycerol, mannitol, sorbitol, sucrose, lactose, maltose, and trehalose.

8. The formulation of claim 1 , further comprising a non-ionic surfactant selected from the group consisting of a polysorbate and a poloxamer.

9. The formulation of claim 1 , further comprising ethylenediaminetetraacetic acid anion (EDTA).

10. The formulation of claim 1 , further comprising at least one salt of a divalent cation selected from the group consisting of MgCl 2 , MgSO 4 , CaCl 2 , CaSO 4 , ZnCl 2 , ZnSO 4 , MnCl 2 , and MnSO 4 .

11. The formulation of claim 1 , further comprising polyvinyl alcohol (PVA).

12. An aqueous formulation comprising either:

(i) an adenovirus vector containing a whole transgene; carboxymethyl cellulose or a salt form thereof at a concentration ranging from about 0.5 mg/mL to about 10 mg/mL; and a combination of TRIS and benzoate ion; and EDTA; wherein the pH of the formulation is about 7; or

(ii) an adenovirus vector containing a whole transgene; carboxymethyl cellulose or a salt form thereof at a concentration ranging from about 0.5 mg/mL to about 10 mg/mL; and a combination of phosphate and citrate ion; wherein the pH of the formulation is about 7.

13. The formulation of claim 1 , wherein the formulation loses less than 1 log infectivity of the starting infectivity when stored for 91 hours at 40° C.

14. The formulation of claim 13 , wherein the log infectivity is measured by a Fluorescence Activated Cell Sorter (FACS) assay or by a Tissue Culture Infectious Dose 50 (TCID 50 ) assay.

15. The formulation of claim 1 , wherein the formulation is a pharmaceutical formulation suitable for administration by injection or infusion.

16. A method for the preparation of a storage stable adenovirus vector aqueous liquid formulation, comprising: forming a mixture of an adenovirus vector containing a whole transgene and carboxymethyl cellulose or a salt form thereof at a concentration ranging from about 0.5 mg/mL to about 10 mg/mL.

17. The formulation of claim 1 , wherein the adenovirus vector is a human adenovirus.

18. The formulation of claim 17 , wherein the human adenovirus is an Ad5 serotype or an Ad35 serotype.

19. The formulation of claim 12 , wherein the adenovirus vector is a human adenovirus.

20. The formulation of claim 19 , wherein the human adenovirus is an Ad5 serotype or an Ad35 serotype.

21. The method of claim 16 , wherein the adenovirus vector is a human adenovirus.

22. The method of claim 21 , wherein the human adenovirus is an Ad5 serotype or an Ad35 serotype.