US2020345812A1PendingUtilityA1
Methods of neuroprotection involving macrophage colony stimulating factor receptor agonists
Est. expiryApr 8, 2031(~4.7 yrs left)· nominal 20-yr term from priority
A61P 25/00A61P 9/10A61K 38/20A61K 38/193A61P 25/16A61P 25/28
66
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Claims
Abstract
The present invention provides methods for preventing, attenuating neuronal damage or stimulating neuronal repair prior or following central nervous system injury.
Claims
exact text as granted — not AI-modified1 . A method of treating a human subject following acute central nervous system injury, the method comprising administering a pharmaceutical composition comprising at least one macrophage colony stimulating factor receptor agonist to said human within a predetermined time period following said acute central nervous system injury.
2 . The method of claim 4 , wherein said acute central nervous system injury is caused by a traumatic brain injury, cerebral ischemia, cerebral glucose deprivation, cerebral oxidative stress, spinal cord injury or excitotoxic injury.
3 . The method of claim 4 , wherein said at least one macrophage colony stimulating factor receptor agonist is macrophage colony stimulating factor.
4 . The method of claim 1 , wherein the method comprises attenuating neuronal damage in the human subject.
5 . The method of claim 1 , wherein the method comprises stimulating neuronal repair in the human subject.
6 . The method of claim 5 , wherein said acute central nervous system injury is caused by a traumatic brain injury, cerebral ischemia, cerebral glucose deprivation, cerebral oxidative stress, spinal cord injury or excitotoxic injury.
7 . The method of claim 5 , wherein said at least one macrophage colony stimulating factor receptor agonist is macrophage colony stimulating factor.
8 . (canceled)
9 . A method of treating a human subject suffering from a chronic central nervous system injury, the method comprising administering a pharmaceutical composition comprising at least one macrophage colony stimulating factor receptor agonist to said human subject following or during said chronic central nervous system injury.
10 . The method of claim 13 , wherein said chronic central nervous system injury is caused by a neurodegenerative disease.
11 . The method of claim 10 , wherein said neurodegenerative disease is Alzheimer's disease, Parkinson's disease, Amyotrophic Lateral Sclerosis or Huntington's disease.
12 . The method of claim 9 , wherein said at least one macrophage colony stimulating factor receptor agonist is macrophage colony stimulating factor.
13 . The method of claim 9 , wherein said method comprises attenuating neuronal damage in the human subject.
14 . The method of claim 9 , wherein the method comprises stimulating neuronal repair in the human subject.
15 . The method of claim 14 , wherein said chronic central nervous system injury is caused by a neurodegenerative disease.
16 . The method of claim 15 , wherein said neurodegenerative disease is Alzheimer's disease, Parkinson's disease, Amyotrophic Lateral Sclerosis or Huntington's disease.
17 . The method of claim 14 , wherein said at least one macrophage colony stimulating factor receptor agonist is macrophage colony stimulating factor.
18 . (canceled)
19 . A method of attenuating or preventing neuronal damage in a human subject at risk of chronic central nervous system injury, the method comprising administering a pharmaceutical composition comprising at least one macrophage colony stimulating factor receptor agonist to said human subject prior to said chronic central nervous system injury.
20 . The method of claim 19 , wherein said chronic central nervous system injury is caused by a neurodegenerative disease.
21 . The method of claim 20 , wherein said neurodegenerative disease is Alzheimer's disease, Parkinson's disease, Amyotrophic Lateral Sclerosis or Huntington's disease.
22 . The method of claim 19 , wherein said at least one macrophage colony stimulating factor receptor agonist is macrophage colony stimulating factor.
23 . (canceled)Join the waitlist — get patent alerts
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