Methods and compositions for the prevention and treatment neuropathy

Patent metadata

Field	Value
Publication number	US-9636378-B2
Application number	US-201314388705-A
Country	US
Kind code	B2
Filing date	Mar 29, 2013
Priority date	Mar 30, 2012
Publication date	May 2, 2017
Grant date	May 2, 2017

Abstract

The disclosure relates to methods for treating a subject suffering from hyperalgesia caused by drug-induced neuropathy by administering to the subject an effective amount of an aromatic-cationic peptide. The disclosure also relates to methods for protecting a subject from hyperalgesia caused by drug-induced neuropathy by administering an effective amount of an aromatic-cationic peptide to a subject at risk for developing the condition.

First claim

What is claimed is:

1. A method for treating peripheral neuropathy or hyperalgesia in a subject in need thereof, comprising administering to the subject an effective amount of a peptide having the formula D-Arg-2′6′-dimethyltyrosine-Lys-Phe-NH 2 .

2. The method of claim 1 , wherein the peripheral neuropathy or hyperalgesia is drug-induced.

3. The method of claim 2 , wherein the drug is a chemotherapeutic agent.

4. The method of claim 3 , wherein the chemotherapeutic agent is procarbazine, nitrofurazone, podophyllum, mustine, ethoglucid, cisplatin, suramin, paclitaxel, chlorambucil, altretamine, carboplatin, cytarabine, docetaxel, dacarbazine, etoposide, ifosfamide with mesna, fludarabine, tamoxifen, teniposide, thioguanine, or vincristine.

5. The method of claim 3 , wherein the chemotherapeutic agent is vincristine.

6. The method of claim 2 , wherein the peptide is administered simultaneous with the drug.

7. The method of claim 2 , wherein the peptide is administered subsequent to the drug.

8. The method of claim 1 , wherein the peripheral neuropathy causes hyperalgesia.

9. The method of claim 1 , wherein the subject is a human.

10. The method of claim 1 , wherein the peptide is administered intravenously, orally, subcutaneously, transdermally, intraperitoneally, intrathecally intramuscularly, intranasally, bucally, sublingually, translingually, or topically.

11. A method for preventing hyperalgesia in a subject in need thereof, comprising administering to the subject an effective amount of a peptide having the formula D-Arg-2′6′-dimethyltyrosine-Lys-Phe-NH 2 .

12. The method of claim 11 , wherein the hyperalgesia is drug-induced.

13. The method of claim 12 , wherein the drug is a chemotherapeutic agent.

14. The method of claim 13 , wherein the chemotherapeutic agent is procarbazine, nitrofurazone, podophyllum, mustine, ethoglucid, cisplatin, suramin, paclitaxel, chlorambucil, altretamine, carboplatin, cytarabine, docetaxel, dacarbazine, etoposide, ifosfamide with mesna, fludarabine, tamoxifen, teniposide, thioguanine, or vincristine.

15. The method of claim 13 , wherein the chemotherapeutic agent is vincristine.

16. The method of claim 12 , wherein the peptide is administered simultaneous with the drug.

17. The method of claim 12 , wherein the peptide is administered subsequent to the drug.

18. The method of claim 11 , wherein the peptide is administered prior the onset of hyperalgesia.

19. The method of claim 11 , wherein the subject is a human.

20. The method of claim 11 , wherein the peptide is administered intravenously, orally, subcutaneously, transdermally, intraperitoneally, intrathecally intramuscularly, intranasally, bucally, sublingually, translingually, or topically.

Assignees

• Stealth Bio Therapeutics Corp
• Stealth Biotherapeutics Corp

Inventors

• Wilson D Travis

Classifications

• A61P39/02

  Antidotes · CPC title

• A61P35/00

  Antineoplastic agents · CPC title

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P25/02

  for peripheral neuropathies · CPC title

• A61P25/04

  Centrally acting analgesics, e.g. opioids · CPC title