Compositions and methods for detection of SMN protein in a subject and treatment of a subject

Patent metadata

Field	Value
Publication number	US-12013403-B2
Application number	US-202117365365-A
Country	US
Kind code	B2
Filing date	Jul 1, 2021
Priority date	Sep 12, 2014
Publication date	Jun 18, 2024
Grant date	Jun 18, 2024

Abstract

Disclosed herein are compounds, compositions and methods for modulating splicing of SMN2 mRNA in a subject. Also provided are uses of disclosed compounds and compositions in the manufacture of a medicament for treatment of diseases and disorders, including spinal muscular atrophy. Also provided are kits for detecting the amount of SMN protein in a sample of cerebrospinal fluid.

First claim

What is claimed is:

1. A method of treating spinal muscular atrophy (SMA) in a human subject in need thereof, the method comprising administering to the human subject by intrathecal bolus injection doses of a pharmaceutical composition comprising a pharmaceutically acceptable carrier and an antisense oligonucleotide consisting of 18 linked nucleosides, wherein the antisense oligonucleotide has a nucleobase sequence consisting of the nucleobase sequence SEQ ID NO:1, wherein each internucleoside linkage of the antisense oligonucleotide is a phosphorothioate linkage, wherein each nucleoside of the antisense oligonucleotide is a 2′-MOE nucleoside, and wherein each cytosine of the antisense oligonucleotide is a 5-methyl cytosine, wherein the doses comprise:
(i) a first dose of 12 mg of the antisense oligonucleotide;
(ii) a second dose of 12 mg of the antisense oligonucleotide administered approximately 12-18 days after administration of the first dose;
(iii) a third dose of 12 mg of the antisense oligonucleotide administered approximately 25-35 days after administration of the first dose, wherein the third dose is administered at least 14 days after the second dose;
(iv) a fourth dose of 12 mg of the antisense oligonucleotide administered approximately 60-70 days after administration of the first dose;
(v) a fifth dose of 12 mg of the antisense oligonucleotide administered approximately 178-188 days after administration of the first dose; and
(vi) a sixth dose of 12 mg of the antisense oligonucleotide administered approximately 298-308 days after administration of the first dose.

2. The method of claim 1 , wherein the administration to the human subject comprises:
(i) the first dose of the antisense oligonucleotide;
(ii) the second dose of the antisense oligonucleotide administered approximately 12 days after administration of the first dose;
(iii) the third dose of the antisense oligonucleotide administered approximately 25 days after administration of the first dose;
(iv) the fourth dose of the antisense oligonucleotide administered approximately 60 days after administration of the first dose;
(v) the fifth dose of the antisense oligonucleotide administered approximately 178 days after administration of the first dose; and
(vi) the sixth dose of the antisense oligonucleotide administered approximately 298 days after administration of the first dose.

3. A method of treating SMA in a human subject in need thereof, the method comprising administering to the human subject by intrathecal bolus injection doses of a pharmaceutical composition comprising a pharmaceutically acceptable carrier and an antisense oligonucleotide consisting of 18 linked nucleosides, wherein the antisense oligonucleotide has a nucleobase sequence consisting of the nucleobase sequence SEQ ID NO:1, wherein each internucleoside linkage of the antisense oligonucleotide is a phosphorothioate linkage, wherein each nucleoside of the antisense oligonucleotide is a 2′-MOE nucleoside, and wherein each cytosine of the antisense oligonucleotide is a 5-methyl cytosine, wherein the doses comprise:
(i) a first dose of 12 mg of the antisense oligonucleotide;
(ii) a second dose of 12 mg of the antisense oligonucleotide administered approximately 15 days after administration of the first dose;
(iii) a third dose of 12 mg of the antisense oligonucleotide administered approximately 29 days after administration of the first dose;
(iv) an additional dose of 12 mg of the antisense oligonucleotide administered approximately 183 days after administration of the first dose; and
(v) an additional dose of 12 mg of the antisense oligonucleotide administered approximately 302 days after administration of the first dose.

4. The method of claim 3 , wherein the human subject is further administered an additional dose of 12 mg of the antisense oligonucleotide approximately 64 days after administration of the first dose.

5. The method of claim 3 , wherein the human subject is administered the antisense oligonucleotide using a spinal anesthesia needle.

6. The method of claim 3 , wherein the antisense oligonucleotide is administered at a concentration of 2.4 mg/mL.

7. The method of claim 6 , wherein the antisense oligonucleotide is administered in an injection volume of 5.0 mL.

8. The method of claim 7 , wherein the human subject has (i) type I SMA; (ii) type II SMA; (iii) type III SMA; or (iv) type IV SMA.

9. The method of claim 7 , wherein the human subject is administered the first dose of the antisense oligonucleotide when the human subject is less than one week old.

10. The method of claim 7 , wherein the human subject is administered the first dose of the antisense oligonucleotide when the human subject is less than one month old.

11. The method of claim 7 , wherein the human subject is administered the first dose of the antisense oligonucleotide when the human subject is less than 3 months old.

12. The method of claim 7 , wherein the human subject is administered the first dose of the antisense oligonucleotide when the human subject is less than 6 months old.

13. The method of claim 7 , wherein the human subject is administered the first dose of the antisense oligonucleotide when the human subject is less than 1 year old.

14. The method of claim 7 , wherein the human subject is administered the first dose of the antisense oligonucleotide when the human subject is less than 2 years old.

15. The method of claim 7 , wherein the human subject is administered the first dose of the antisense oligonucleotide when the human subject is less than 15 years old.

16. The method of claim 7 , wherein the human subject is administered the first dose of the antisense oligonucleotide when the human subject is older than 15 years old.

17. The method of claim 3 , wherein the human subject is a human subject having one or more symptoms associated with spinal muscular atrophy.

Assignees

• Biogen Ma Inc

Inventors

• Rigo Frank
• Bishop Katherine M

Classifications

• G01N2800/28

  Neurological disorders · CPC title

• G01N2333/47

  Assays involving proteins of known structure or function as defined in the subgroups · CPC title

• C12N2320/35

  based on a specific dosage / administration regimen · CPC title

• C12N2320/32

  Special delivery means, e.g. tissue-specific · CPC title

• C12N2310/3341

  5-Methylcytosine · CPC title