METHODS OF TREATING NEUROPATHIC PAIN
The disclosure relates, at least in part, to methods of treating neuropathic pain in a patient in need thereof by administering an effective amount of a disclosed compound, e.g. a peptide NMDA receptor partial agonist.
1 . A method for treating neuropathic pain in a patient in need thereof, comprising administering to said patient a pharmaceutically effective amount of a peptide that modulates a glycine site on a NMDA receptor.
2 . The method of claim 1 , wherein the neuropathic pain is associated with a condition selected from the group consisting of herpes, HIV, traumatic nerve injury, stroke, postischemia, fibromyalgia, reflex sympathetic dystrophy, complex regional pain syndrome, spinal cord injury, sciatica, phantom limb pain, diabetic neuropathy, and cancer chemotherapeutic-induced neuropathic pain.
3 . The method of claim 1 , wherein the NMDA receptor modulating peptide is represented by:
or pharmaceutically acceptable salts thereof.
4 . The method of claim 1 , wherein the peptide is administered intravenously, intraperitoneally, intramuscularly, or subcutaneously.
5 . The method of claim 1 , wherein the method comprises administering a single-dose of said peptide.
6 . The method of claim 1 , wherein about 1 day after administration the patient has substantial improvement in neuropathic pain.
7 . The method of claim 1 , wherein about 8 days after administration the patient has substantial improvement in neuropathic pain.
8 . The method of claim 1 , wherein the compound is administered daily.
9 . The method of claim 1 , wherein upon said administration, the patient has no significant axatia.
10 . The method of claim 1 , wherein the pharmaceutically effective amount is about 0.01 mg/kg to about 1000 mg/kg.
11 . A method of treating neuropathic pain in a patient in need thereof, comprising administering to said patient a single dose of a compound represented by:
or pharmaceutically acceptable salts thereof, wherein after 1 day the patient has substantial improvement in neuropathic pain.
12 . The method of claim 11 , wherein after 8 days the patient has substantial improvement in neuropathic pain.
13 . The method of claim 11 , wherein the single dose comprises about 0.01 mg/kg to about 1000 mg/kg.
14 . A method of treating neuropathic pain in a patient in need thereof, comprising administering to said patient an effective amount of SEQ ID. NO: 13 (Thr--Pro--Pro-Thr).