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Last Updated: May 10, 2024

Claims for Patent: 5,932,611


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Summary for Patent: 5,932,611
Title: Angiogenesis inhibitor for the treatment of cancer
Abstract:The present invention provides a treatment for angiogenic diseases, including solid tumors. The treatment consists of administering therapeutically active dosages of FC101, resulting in a reduction in endothelial cell proliferation and inhibition of new blood vessel formation. FC101 can also be used as a lead compound to develop other pharmacologically-active compounds, by adding or substituting different functional groups for those already present on the FC101 molecule.
Inventor(s): Wuthier; Roy E. (Columbia, SC), Nie; Daotai (Detroit, MI)
Assignee: University of South Carolina (Columbia, SC)
Application Number:08/975,813
Patent Claims:1. A method for treating cancer sensitive to the compounds below in a patient, comprising administering to said patient a therapeutically active dosage of a composition comprising 5-amino-2,2-dimethyl-6-[3'-(R,S) amino-4'-hydroxy-butan-1-one]-2,3-dihydro-4H-1-benzopyran-4-one, wherein said composition is administered via a pharmaceutically or veterinarily acceptable carrier, for a time effective to treat said cancer by inhibiting the formation of new blood vessels in said patient.

2. A method according to claim 1, wherein said therapeutically active dosage is in the range of about 0.2 .mu.g to about 200 g.

3. A method according to claim 1, wherein said composition is administered via a mucosal route.

4. A method according to claim 1, wherein said composition is administered via a parenteral route.

5. A method according to claim 1, wherein said cancer is a solid tumor sensitive to said compounds.

6. A method according to claim 1, wherein said pharmaceutically or veterinarily acceptable carrier is chosen from the group consisting of saline, glucose, sterile water and mixtures thereof.

7. A method for inhibiting metastasis sensitive to the compounds below in a patient comprising administering to said patient a therapeutically active dosage of a composition comprising 5-amino-2,2-dimethyl-6-[3'-(R,S) amino4'-hydroxy-butan-1-one]-2,3-dihydro-4H-1-benzopyran-4-one, wherein said composition is administered via a pharmaceutically or veterinarily acceptable carrier, for a time effective to inhibit said metastasis by inhibiting the formation of new blood vessels.

8. A method according to claim 7, wherein said therapeutically active dosage is in the range of about 0.2 .mu.g to about 200 g.

9. A method according to claim 7, wherein said composition is administered via a mucosal route.

10. A method according to claim 7, wherein said composition is administered via a parenteral route.

11. A method according to claim 7, wherein said pharmaceutically or veterinarily acceptable carrier is chosen from the group consisting of saline, glucose, sterile water and mixtures thereof.

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