IP Library Granted Patent US 8,912,184
Granted Patent B1
US 8,912,184 · App. 13/235,221 · Granted Dec 16, 2014

Therapeutic and diagnostic methods

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Quick Facts
Patent No.
US 8,912,184
App. No.
13/235,221
Granted
Dec 16, 2014
Kind
B1
Abstract

The invention relates to methods of treating diseases, particularly cancers, that respond favorably to the inhibition of Nicotinamide phosphoribosyltransferase (Nampt); it also relates to therapeutic methods that utilize Nampt inhibitors in combination with NAD biosynthesis precursors to intentionally kill cancer cells while limiting or minimizing toxicity to normal host cells; and it relates to methods of identifying cancers that will be most responsive to treatment with Nampt inhibitors, particularly when administered in combination with nicotinic acid.

Claims (21)

1. A method of treating cancers associated with low level expression of nicotinic acid phosphoribosyltransferase 1 (Naprt1), comprising:

identifying a cancer associated with a low level of Naprt1 expression; and

administering to a subject in need thereof, a composition comprising a therapeutically effective amount of a compound of Formulae I-IVc or a compound of Tables 1 or 2, or a pharmaceutically acceptable salt thereof.

2. The method of claim 1 , wherein identifying a cancer associated with a low level of Naprt1 expression comprises determining the level of expression of Naprt1 protein in cells of the cancer.

3. The method of claim 2 , wherein determining the level of expression of Naprt1 protein is by way of a Western Blot.

4. The method of claim 2 , wherein determining the level of expression of Naprt1 protein is by way of an Enzyme-Linked Immunosorbant Assay (ELISA).

5. The method of claim 1 , wherein identifying a cancer associated with a low level of Naprt1 expression comprises determining the level of expression of the mRNA transcript encoding the Naprt1 protein in cells of the cancer.

6. The method of claim 5 , wherein determining the level of expression of the mRNA transcript encoding the Naprt1 protein is by way of a Northern Blot.

7. The method of claim 5 , wherein determining the level of expression of the mRNA transcript encoding the Naprt1 protein is by way of quantitative RT-PCR.

8. The method of claim 1 , wherein said cancer is associated with low expression levels of nicotinamide phosphoribosyltransferase (Nampt).

9. The method of claim 8 , further comprising determining whether said cancer expresses low levels of the Nampt.

10. The method of claim 1 , further comprising determining whether said cancer is associated with nicotinic acid (NA) Rescue Phenotype.

11. The method of claim 10 , wherein said cancer is associated with NA Rescue Phenotype.

12. The method of claim 1 , further comprising administering nicotinic acid to said subject.

13. A method of treating cancers associated with low level expression of nicotinic acid phosphoribosyltransferase 1 (Naprt1), comprising:

identifying a cancer associated with a low level of Naprt1 expression,

administering to a subject in need thereof, a composition comprising a therapeutically effective amount of: (i) nicotinic acid; (ii) a compound of Formulae I-IVc or a compound of Tables 1 or 2, or a pharmaceutically acceptable salt thereof.

14. The method of claim 13 , wherein said nicotinic acid is administered prior to the therapeutically effective amount of a compound of Formulae I-Formulae I-IVc or a compound of Tables 1 or 2, or a pharmaceutically-acceptable salt thereof.

15. The method of claim 13 , wherein said nicotinic acid is administered at the same time as the therapeutically effective amount of a compound of Formulae I-IVc or a compound of Tables 1 or 2, or a pharmaceutically-acceptable salt thereof.

16. The method of claim 13 , wherein said nicotinic acid is administered after the therapeutically effective amount of a compound of Formulae I-IVc or a compound of Tables 1 or 2, or a pharmaceutically-acceptable salt thereof.

17. The method of claim 16 , wherein said nicotinic acid is administered as part of the same dosage form comprising the therapeutically effective amount of a compound of Formulae I-IVc or a compound of Tables 1 or 2, or a pharmaceutically-acceptable salt thereof.

Assignments (6)
LIEN Recorded Jan 9, 2017
From: STOEL RIVES LLP
To: SUNFLOWER RESEARCH LLC
Reel/Frame 040900/0229 →
LIEN Recorded May 20, 2015
From: SUNFLOWER RESEARCH LLC
To: STOEL RIVES LLP
Reel/Frame 035749/0755 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2015
From: SEXTON, RONALD
To: SUNFLOWER RESEARCH LLC
Reel/Frame 034992/0218 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 26, 2015
From: ALZHEIMER'S INSTITUTE OF AMERICA, INC.
To: SEXTON, RONALD
Reel/Frame 034814/0046 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 13, 2014
From: MYREXIS, INC.
To: ALZHEIMER'S INSTITUTE OF AMERICA, INC.
Reel/Frame 034235/0701 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2012
From: FLEISCHER, TRACEY C.; CIMBORA, DANIEL M.; FLICK, JEFFREY S.; GASSMAN, ANDREW D.; BAICHWAL, VIJAY R.; PAPAC, DAMON I.
To: MYREXIS, INC.
Reel/Frame 028097/0120 →