US2008279814A1PendingUtilityA1
Methods of treating neurological conditions with hematopoeitic growth factors
Est. expiryDec 31, 2022(expired)· nominal 20-yr term from priority
Inventors:Wolf-Ruediger SchaebitzArmin SchneiderCarola KruegerClemens SommerStefan SchwabRainer KollmarMartin MaurerDaniela WeberNikolaus Gassler
A61P 9/10A61P 9/00A61P 25/28A61P 25/22A61P 25/24A61P 25/14A61P 25/00A61P 25/16A61K 38/49G01N 33/5058G01N 33/5008G01N 33/5023A61K 38/193G01N 33/5041A61P 21/00G01N 33/6872
55
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Claims
Abstract
The present invention relates to a method of treating a neurological condition in a mammal by administering at least one hematopoietic growth factor.
Claims
exact text as granted — not AI-modified1 . A method of treating a neurological condition in a mammal, comprising administering to the mammal in need thereof, a hematopoietic factor selected from the group consisting of IL-5, a derivative thereof, a mimetic thereof, and a combination thereof in an amount sufficient to treat the neurological condition.
2 . The method of claim 1 , wherein said neurological condition is selected from the group consisting of a neurological disease with pathophysiological mechanisms involving ischemia, a neurological disease with pathophysiological mechanisms involving hypoxia, a neurodegenerative disease, and a disease of the nervous system accompanied by neural cell death.
3 . The method of claim 1 , wherein the neurological condition is neurological disease with pathophysiological mechanisms involving ischemia or hypoxia.
4 . The method of claim 3 , wherein the neurological disease with pathophysiological mechanisms involving ischemia or hypoxia is stroke.
5 . The method of claim 1 , further comprising administering one or more additional hematopoietic factors.
6 . The method of claim 1 , wherein the neurological condition is a psychiatric condition.
7 . The method of claim 6 , wherein the psychiatric condition is depression.
8 . The method of claim 1 , wherein the neurological condition is a dementia or multiple sclerosis.
9 . (canceled)
10 . (canceled)
11 . The method of claim 1 , wherein the neurological condition is stroke, Parkinson's disease, amyotrophic lateral sclerosis, neurotrauma, cerebral ischemia due to cardiac arrest, cerebral ischemia during an operative procedure, multiple sclerosis, Huntington's disease, glaucoma, neuropathy, a lysosomal storage disease, or spinal cord injury.
12 . (canceled)
13 . (canceled)
14 . The method of claim 1 , which further comprises administering a hemodynamically active compound.
15 . The method of claim 1 , which further comprises administering tissue plasminogen activator to the mammal.
16 . The method of claim 1 , which further comprises administering an agent that facilitates passage over the blood brain barrier.
17 . The method of claim 1 , which further comprises administering an anti-apoptotic agent.
18 . The method of claim 15 , wherein the neurological condition is stroke.
19 . The method of claim 10 , further comprising administering tissue plasminogen activator to the mammal.
20 . The method of claim 1 , wherein the hematopoietic factor is a human factor or derived from a human factor.
21 . The method of claim 1 , wherein the mammal is human.
22 . The method of claim 1 , wherein the hematopoietic factor is administered by one or more modes of administration selected from the group consisting of direct intracerebral injection, intravenously, intraarterially, orally, and subcutaneously.
23 - 55 . (canceled)
56 . A method for enhancing the cognitive ability of a mammal in need thereof, comprising administering a hematopoietic factor selected from the group consisting of IL-3, IL-5, a derivative thereof, a mimetic thereof, and a combination thereof in an amount sufficient to enhance the cognitive ability of a mammal relative to the mammal prior to the administrating.
57 . The method of claim 56 , wherein the mammal is a human.Cited by (0)
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