Highly potent acid alpha-glucosidase with enhanced carbohydrates
View Patent ↗Recombinant human alpha glucosidase (rhGAA) composition derived from CHO cells that contains a more optimized glycan composition consisting of a higher amount of rhGAA containing N-glycans carrying mannose-6-phosphate (M6P) or bis-M6P than conventional rhGAAs, along with low amount of non-phosphorylated high mannose glycans, and low amount of terminal galactose on complex oligosaccharides. Compositions containing the rhGAA, and methods of use are described.
1. A composition comprising recombinant human acid alpha-glucosidase (rhGAA) produced from Chinese hamster ovary (CHO) cells, wherein 40%-60% of the N-glycans on the rhGAA are complex type N-glycans; and wherein the rhGAA comprises 3.0-5.0 mol mannose-6-phosphate (M6P) residues per mol rhGAA.
2. The composition of claim 1 , wherein the rhGAA comprises 3.0 to 4.0 mol M6P per mol rhGAA.
3. The composition of claim 1 , wherein the rhGAA comprises 4.0 to 5.0 mol M6P per mol rhGAA.
4. The composition of claim 1 , wherein the rhGAA further comprises at least 4 mol sialic acid per mol rhGAA.
5. The composition of claim 1 , wherein the rhGAA further comprises 2.0 to 8.0 mol sialic acid residues per mol of rhGAA.
6. The composition of claim 1 , wherein the composition further comprises a pharmacological chaperone.
7. The composition of claim 1 , wherein the rhGAA comprises at least one bis-phosphorylated N-glycan per rhGAA.
8. The composition of claim 1 , wherein about 45%-55% of the N-glycans on the rhGAA are complex type N-glycans.
9. The composition of claim 1 , wherein 50% of the N-glycans on the rhGAA are complex type N-glycans.
10. The composition of claim 1 , wherein the rhGAA comprises 4 mol M6P per mol rhGAA, 4.5 mol sialic acid per mol rhGAA, and at least one bis-phosphorylated N-glycan per rhGAA.
11. The composition of claim 10 , wherein the composition further comprises the pharmacological chaperone N-butyl-deoxynojirimycin or a pharmaceutically acceptable salt thereof.
12. A method for treating Pompe disease in a subject in need thereof, the method comprising administering the composition of claim 1 to the subject in an amount sufficient to treat Pompe disease.
13. The method of claim 12 , wherein said composition is administered to cardiac muscle of the subject.
14. The method of claim 12 , wherein said composition is administered to quadriceps, triceps, or other skeletal muscle of the subject.
15. The method of claim 12 , wherein said composition is administered to the diaphragm of the subject.
16. The method of claim 12 , wherein said composition is combined with a pharmacological chaperone, and wherein said composition and said pharmacological chaperone are either administered as a single pharmaceutical composition or administered separately.
17. The method of claim 12 , wherein said composition is combined with 1-deoxynojirimycin or a pharmaceutically acceptable salt thereof, and wherein said composition and said 1-deoxynojirimycin or pharmaceutically acceptable salt thereof are either administered as a single pharmaceutical composition or administered separately.
18. The method of claim 12 , wherein said composition is combined with N-butyl-deoxynojirimycin or a pharmaceutically acceptable salt thereof, and wherein said composition and said N-butyl-deoxynojirimycin or pharmaceutically acceptable salt thereof are either administered as a single pharmaceutical composition or administered separately.