Patent · US Active

Compositions and methods for delivering clonidine and bupivacaine to a target tissue site

US8623396B2 · kind B2 · utility

13Cited by
39References
20Claims
0Family size

Assignee

Inventors

Key dates

Filing dateDec 2, 2011
Grant dateJan 7, 2014
Priority date
Expiry dateDec 28, 2031

Classification

  • Technology area (CPC A)Human Necessities
  • CPC primaryA61P29/00
  • WIPO fieldPharmaceuticals
  • WIPO sectorChemistry

Abstract

Effective treatments of pain for extended periods of time are provided. Through the administration of an effective amount of immediate release bupivacaine or lidocaine and a sustained release clonidine at or near a target site, one can relieve pain caused by diverse sources, including but not limited to spinal disc herniation (i.e. sciatica), spondilothesis, stenosis, discogenic back pain and joint pain. When appropriate formulations are provided within biodegradable polymers, this relief can be continued for at least three days. In some embodiments, the relief can be for at least twenty-five days, at least fifty days, at least one hundred days, at least one hundred and thirty-five days or at least one hundred and eighty days or longer.

Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.