US2020368318A1PendingUtilityA1
Compositions and methods for treatment during non-acute periods following cns neurological injury
Est. expiryAug 15, 2028(~2.1 yrs left)· nominal 20-yr term from priority
A61K 38/18A61P 25/00A61K 38/00A61P 9/10A61K 38/1808A61K 38/1883A61P 25/28
64
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Claims
Abstract
This invention relates to treatment of neuroinjury in a post-acute window or in a chronic period following neuroinjury.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for administering a polypeptide comprising an epidermal growth factor-like (EGF-like) domain to a mammal, said method comprising: administering a polypeptide comprising an epidermal growth factor-like (EGF-like) domain following neuroinjury in said mammal; and, initiating the administering at least two days after the neuroinjury.
2 . A method of claim 1 , wherein said initiating step begins at a three days after the neuroinjury.
3 . The method of claim 1 , wherein said initiating step begins at least seven days after the neuroinjury.
4 . A method of claim 1 wherein the EGF-like domain is encoded by the neuregulin (NRC)-1 gene, (NRG)-2 gene, (NRG)-3 gene, (NRC)-4 gene.
5 . The method of claim 1 , wherein said polypeptide is OGF2.
6 . The method of claim 1 , wherein said mammal is a human
7 . A method for administering a polypeptide comprising an epidermal growth factor-like (EGF-like) domain to a mammal, said method comprising:
administering a polypeptide comprising an epidermal growth factor-like (EGF-like) domain following neuroinjury in said mammal; initiating the administering at within six hours after the neuroinjury; and, continuing the administering step into a time period more than six hours post injury.
8 . The method of claim 7 , wherein the continuing step comprises continuing the administering step into a time period more than 48 hours post injury.
9 . The method of claim 7 , wherein the continuing step comprises continuing the administering step into a time period more than 72 hours post injury.
10 . A method of claim 7 wherein the EGF-like domain is encoded by the neuregulin (NRG)-1 gene, (NRG)-2 gene, (NRG)-3 gene, (NRG)-4 gene.
11 . The method of claim 7 , wherein said polypeptide is GGF2.
12 . The method of claim 7 , wherein said mammal is a human.
13 . A method for administering a polypeptide comprising an epidermal growth factor-like (EGF-like) domain following an ischemic central nervous system neuroinjury in a mammal, said method comprising:
administering the peptide following neuroinjury in said mammal; and, initiating the administering after the mammal has achieved a complete post-injury ischemic lesion cell death volume.
14 . A method of claim 13 , wherein the EGF-like domain is encoded by the neuregulin (NRG)-1 gene, (NRG)-2 gene, (NRG)-3 gene, (NRG)-4 gene.
15 . The method of claim 13 , wherein said polypeptide is GGF2.Join the waitlist — get patent alerts
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