US2006216276A1PendingUtilityA1
Use of materials for treatment of central nervous system lesions
Est. expiryMar 7, 2025(expired)· nominal 20-yr term from priority
A61P 9/10A61K 35/30A61P 25/00
50
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Disclosed are methods and materials for treatment of central nervous system lesions. Preferred methods and materials comprise neuronal precursor cells and/or marrow adherent stem cell-derived neuronal cells.
Claims
exact text as granted — not AI-modified1 . A method comprising:
providing neuronal precursor cells; and administering the neuronal precursor cells to a patient suffering from a central nervous system lesion in an amount sufficient to facilitate functional recovery of the patient.
2 . The method of claim 1 , wherein the neuronal precursor cells are administered locally.
3 . The method of claim 2 , wherein the neuronal precursor cells are administered to a central nervous system lesion of the patient.
4 . The method of claim 1 , wherein the neuronal precursor cells are administered intraparenchymally.
5 . The method of claim 1 , wherein the neuronal precursor cells comprise human neuronal precursor cells.
6 . The method of claim 1 , wherein providing neuronal precursor cells comprises:
providing marrow adherent stem cells; transdifferentiating the marrow adherent stem cells into neuronal precursor cells.
7 . The method of claim 1 , wherein the central nervous system lesion is caused by ischemic stroke or hemorrhagic stroke.
8 . The method of claim 1 , further comprising
allowing the neuronal precursor cells to migrate from a site of administration to other locations in the patient.
9 . The method of claim 8 , wherein another location in the patient comprises a central nervous system lesion.
10 . The method of claim 1 , further comprising
administering an immunosuppressive agent to the patient.
11 . The method of claim 1 , wherein the functional recovery is a partial functional recovery.
12 . The method of claim 1 , wherein the neuronal precursor cells are allogeneic with respect to the patient.
13 . A graft forming unit comprising:
neuronal precursor cells present in an amount sufficient to facilitate functional recovery of a patient suffering from a central nervous system lesion following administration of the neuronal precursor cells to the patient; and a pharmaceutically acceptable carrier.
14 . The graft forming unit of claim 13 , wherein the pharmaceutically acceptable carrier comprises a solvent, a dispersion media, an antibacterial agents, or an antifungal agent.
15 . The graft forming unit of claim 13 , wherein the graft comprises neuronal precursor cells in an amount ranging from about 10,000 to about 100 million neuronal precursor cells.
16 . The graft forming unit of claim 13 , wherein the neuronal precursor cells comprise a label.
17 . The graft forming unit of claim 13 , wherein the neuronal precursor cells comprise human neuronal precursor cells.
18 . A method comprising:
providing marrow-adherent stem cell-derived neuronal cells; and administering the marrow-adherent stem cell-derived neuronal cells to a patient suffering from a central nervous system lesion in an amount sufficient to facilitate functional recovery of the patient.
19 . The method of claim 18 , wherein the marrow-adherent stem cell-derived neuronal cells are administered locally.
20 . The method of claim 19 , wherein the marrow-adherent stem cell-derived neuronal cells are administered to a central nervous system lesion of the patient.
21 . The method of claim 18 , wherein the marrow-adherent stem cell-derived neuronal cells are administered intraparenchymally.
22 . The method of claim 18 , wherein the marrow-adherent stem cell-derived neuronal cells comprise human marrow-adherent stem cell-derived neuronal cells.
23 . The method of claim 18 , wherein providing marrow-adherent stem cell-derived neuronal cells comprises:
providing marrow adherent stem cells; and inducing the marrow adherent stem cells to form marrow-adherent stem cell-derived neuronal cells.
24 . The method of claim 23 , further comprising:
transdifferentiating the marrow adherent stem cells into neuronal precursor cells; and inducing the neuronal precursor cells to form neuronal cells.
25 . The method of claim 18 , wherein the central nervous system lesion is caused by ischemic stroke or hemorrhagic stroke.
26 . The method of claim 18 , further comprising administering an immunosuppressive agent to the patient.
27 . The method of claim 18 , wherein the functional recovery is a partial functional recovery.
28 . The method of claim 18 , wherein the marrow-adherent stem cell-derived neuronal cells are allogeneic with respect to the patient.
29 . A graft forming unit comprising:
marrow-adherent stem cell-derived neuronal cells present in an amount sufficient to facilitate functional recovery of a patient suffering from a central nervous system lesion following administration of the marrow-adherent stem cell-derived neuronal cells to the patient; and a pharmaceutically acceptable carrier.
30 . The graft forming unit of claim 29 , wherein the pharmaceutically acceptable carrier comprises a solvent, a dispersion media, an antibacterial agents, or an antifungal agent.
31 . The graft forming unit of claim 29 , wherein the graft comprises neuronal precursor cells in an amount ranging from about 10,000 to about 100 million neuronal precursor cells.
32 . The graft forming unit of claim 29 , wherein the marrow-adherent stem cell-derived neuronal cells comprise a label.
33 . The graft forming unit of claim 29 , wherein the marrow-adherent stem cell-derived neuronal cells comprise human marrow-adherent stem cell-derived neuronal cells.Join the waitlist — get patent alerts
Track US2006216276A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.