Deoxyribonucleoside monophospate bypass therapy for mitochondrial DNA depletion syndrome

Patent metadata

Field	Value
Publication number	US-11633418-B2
Application number	US-202117242862-A
Country	US
Kind code	B2
Filing date	Apr 28, 2021
Priority date	Mar 26, 2015
Publication date	Apr 25, 2023
Grant date	Apr 25, 2023

Abstract

The invention relates generally to a pharmacological therapy for a human genetic diseases, specifically mitochondrial DNA depletion syndromes, and more specifically, thymidine kinase 2 (TK2) deficiency. The pharmacological therapy involves the administration of at least one deoxyribonucleoside monophosphate, or mixtures thereof. For the treatment of TK2 deficiency, the pharmacological therapy involves the administration of either deoxythymidine monophosphate (dTMP) or deoxycytidine monophosphate (dCMP), or mixtures thereof. This molecular bypass approach is applicable to other disorders of unbalanced nucleotide pools, especially those found in mitochondrial DNA depletion syndrome.

First claim

The invention claimed is:

1. A method of treating thymidine kinase 2 (TK2) deficiency in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a composition comprising deoxythymidine monophosphate (dTMP) and deoxycytidine monophosphate (dCMP), wherein the therapeutically effective amount is about 100 mg/kg/day of total deoxyribonucleoside monophosphaste in the composition and the composition is administered to the subject parenterally.

2. The method of claim 1 , wherein the parenteral administration is intravenous administration.

3. The method of claim 1 , wherein the composition is administered once a day, twice a day, three times a day, four times a day, five times daily or six times daily.

4. The method of claim 3 , wherein the therapeutically effective amount of the composition per administration is between about 15 mg/kg to about 20 mg/kg.

5. A method of treating mitochondrial DNA depletion syndrome in a human subject in need thereof comprising administering to the subject a therapeutically effective amount of a composition comprising at least one deoxyribonucleoside monophosphate wherein the mitochondrial DNA depletion syndrome is characterized by at least one mutation in a gene chosen from the group consisting of: DGUOK; TYMP; and RRM2B, and wherein the therapeutically effective amount is about 100 mg/kg/day of total deoxyribonucleoside monophosphate in the composition and the composition is administered to the subject parenterally.

6. The method of claim 5 , wherein the parenteral administration is intravenous administration.

7. The method of claim 5 , wherein the composition is administered, once a day, twice a day, three times a day, four times a day five times daily or six times daily.

8. The method of claim 7 , wherein the therapeutically effective amount of the composition per administration is between about 15 mg/kg to about 20 mg/kg.

9. A method of treating mitochondrial DNA depletion syndrome in a human subject in need thereof comprising administering to the subject a therapeutically effective amount of a composition comprising at least one deoxyribonucleoside monophosphate wherein the mitochondrial DNA depletion syndrome is characterized by at least one mutation in a gene chosen from the group consisting of: TK2, DGUOK; TYMP; and RRM2B, and wherein the therapeutically effective amount is about 100 mg/kg/day of total deoxyribonucleoside monophosphate in the composition and the composition is administered to the subject intrathecally.

10. The method of claim 9 , wherein the composition is administered, once a day, twice a day, three times a day, four times a day five times daily or six times daily.

11. The method of claim 10 , wherein the therapeutically effective amount of the composition per administration is between about 15 mg/kg to about 20 mg/kg.

Assignees

• Univ Columbia
• Univ Columbia

Inventors

• Hirano Michio
• Garone Caterina

Classifications

• A61K31/708

  having oxo groups directly attached to the purine ring system, e.g. guanosine, guanylic acid · CPC title

• A61K31/7072 Primary

  having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine · CPC title

• A61K31/7068

  having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid · CPC title

• A61K31/7076

  containing purines, e.g. adenosine, adenylic acid · CPC title