IP Library › Granted Patent US 10,456,454
Granted Patent B2
US 10,456,454 · App. 15/016,141 · Granted Oct 29, 2019

CNS delivery of therapeutic agents

Inventors: Pericles Calias (Melrose, MA); Jing Pan (Boxborough, MA); Jan Powell (Concord, MA); Lawrence Charnas (Natick, MA); Thomas McCauley (Cambridge, MA); Teresa Leah Wright (Lexington, MA); Richard Pfeifer (North Granby, CT); Zahra Shahrokh (Weston, MA)
Assignee: Shire Human Genetic Therapies, Inc.
A61K38/47A61K9/0019A61K9/0085A61K9/08A61K9/19A61K35/76A61K35/761A61K38/46A61K38/465A61K47/02A61K47/26C07K14/65C12N9/2402C12N9/2437C12Y301/06008C12Y301/06013C12Y302/0105C12Y302/01045C12Y302/01046C12Y310/01001
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Quick Facts
Patent No.
US 10,456,454
App. No.
15/016,141
Granted
Oct 29, 2019
Kind
B2
Abstract

The present invention provides an effective and less invasive approach for direct delivery of therapeutic agents to the central nervous system (CNS). In some embodiments, the present invention provides methods including a step of administering intrathecally to a subject suffering from or susceptible to a lysosomal storage disease associated with reduced level or activity of a lysosomal enzyme, a composition comprising a replacement enzyme for the lysosomal enzyme.

Claims (27)

1. A formulation for intrathecal administration comprising a lysosomal enzyme at a concentration at or greater than about 5 mg/ml, and a surfactant, wherein the formulation comprises phosphate at a concentration of no greater than 50 mM.

2. The formulation of claim 1 , wherein the lysosomal enzyme is present at a concentration ranging from about 10-100 mg/ml.

3. The formulation of claim 1 , wherein the lysosomal enzyme is present at a concentration ranging from about 10-50 mg/ml.

4. The formulation of claim 1 , wherein the lysosomal enzyme is present at a concentration of about 10 mg/ml.

5. The formulation of claim 1 , wherein the lysosomal enzyme is present at a concentration of about 30 mg/ml.

6. The formulation of claim 1 , wherein the phosphate is present at a concentration no greater than 25 mM.

7. The formulation of claim 1 , wherein the phosphate is present at a concentration no greater than 10 mM.

8. The formulation of claim 1 , wherein the phosphate is present at a concentration no greater than 5 mM.

9. The formulation of claim 1 , further comprising a tonicifier.

10. The formulation of claim 9 , wherein the tonicifier is salt.

11. The formulation of claim 10 , wherein the salt is NaCl.

12. The formulation of claim 11 , wherein the NaCl is present at a concentration no greater than 300 mM.

13. The formulation of claim 12 , wherein the NaCl is present at a concentration ranging from 137-154 mM.

14. The formulation of claim 13 , wherein the NaCl is present at a concentration of 154 mM.

15. The formulation claim 1 , wherein the surfactant is a polysorbate surfactant.

16. The formulation claim 15 , wherein the polysorbate surfactant is selected from the group consisting of polysorbate 20, polysorbate 40, polysorbate 60, polysorbate 80 and combinations thereof.

17. The formulation of claim 16 , wherein the polysorbate surfactant is polysorbate 20.

18. The formulation of claim 17 , wherein the polysorbate 20 is present at a concentration no greater than 0.02%.

19. The formulation of claim 18 , wherein the polysorbate 20 is present at a concentration of 0.005%.

20. The formulation of claim 1 , further comprising a buffering agent.

21. The formulation of claim 20 , wherein the buffering agent is selected from the group consisting of acetate, histidine, succinate, Tris, and combinations thereof.

22. The formulation of claim 1 , wherein the formulation has a pH of approximately 3-8.

23. The formulation of claim 22 , wherein the formulation has a pH of approximately 5.5-6.5.

24. The formulation of claim 23 , wherein the formulation has a pH of approximately 6.0.

25. The formulation of claim 1 , wherein the formulation is present in a volume of less than about 3 ml.

26. The formulation of claim 1 , wherein the formulation is a liquid formulation.

27. The formulation of claim 1 , wherein the formulation is formulated as lyophilized dry powder.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2022
From: SHIRE HUMAN GENETIC THERAPIES, INC.
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 061447/0760 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2016
From: CALIAS, PERICLES; PAN, JING; POWELL, JAN; CHARNAS, LAWRENCE; MCCAULEY, THOMAS; WRIGHT, TERESA LEAH; PFEIFER, RICHARD; SHAHROKH, ZAHRA
To: SHIRE HUMAN GENETIC THERAPIES, INC.
Reel/Frame 038334/0132 →
Continuity (9)
Division 13168961 · Jun 25, 2011
Provisional Application 61358857 · Jun 25, 2010
Provisional Application 61360786 · Jul 1, 2010
Provisional Application 61387862 · Sep 29, 2010
Provisional Application 61435710 · Jan 24, 2011
Provisional Application 61442115 · Feb 11, 2011
Provisional Application 61476210 · Apr 15, 2011
Provisional Application 61495268 · Jun 9, 2011
Related Publication 20170042978A1 · Feb 16, 2017
Cited By (1)
US 12,409,210