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Peripherally-Acting Cannabinoid Receptor Agonists for Chronic Pain


技術優勢

No centrally-mediated side effectsHigh affinity for cannabinoid receptors


技術應用

Control chronic pain of inflammatory and neuropathic originReduce intraocular pressure


詳細技術說明

Dr. Igor Spigelman of UCLA’s School of Dentistry and Dr. Herbert Seltzman, a collaborator at RTI International, have designed small molecules effective in alleviating chronic pain of inflammatory and neuropathic origin without any centrally-mediated side effects. The molecules are peripherally-acting cannabinoid compounds with high affinity for cannabinoid receptors and have been specifically designed to have limited permeability at the blood-brain barrier.


申請號碼

9656981


其他

State Of Development

  • Compounds with high agonist activity for CB1R and low BBB permeability were examined for stability in blood plasma
  • Pharmacokinetic studies support minimal brain penetration
  • Preclinical trials in rat models of chronic inflammatory and neuropathic pain have been completed and lead compounds have been identified

Background

Current treatments of different types of chronic pain are geared towards decreasing inflammation (if it exists) and maximizing pain relief while minimizing side effects associated with each particular drug type. Unfortunately, this has been a difficult goal to achieve and all of the current treatments for chronic pain, particularly pain of neuropathic origin, have significant side effects which limit their usefulness. Recently, drugs targeting cannabinoid receptors have proven efficacious for patients. However, while current clinical treatments with FDA-approved cannabinoid-based analgesic can provide relief from chronic pain symptoms, these treatments also produce several significant central nervous system-mediated side effects. 


Tech ID/UC Case

23480/2012-715-0


Related Cases

2012-715-0


國家/地區

美國

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