Treatment of demyelinating diseases

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai

Reexamination Certificate

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Details

C514S114000, C514S221000, C514S234200, C514S248000, C514S249000, C514S250000, C514S378000

Reexamination Certificate

active

10398876

ABSTRACT:
This invention relates to methods for the treatment or prevention of central nervous system (CNS) cell damage and functional damage in mammals due to demyelinating disease including multiple sclerosis. More specifically, the invention comprises a method of treating a demyelinating disease of the CNS in a mammal, the method comprising co-administering to the mammal, either sequentially or simultaneously, GPE or analogues or peptidomimetics or a prodrug thereof, or a pharmaceutically acceptable salt thereof, and an AMPA (α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate)/kainate antagonist, or a pharmaceutically acceptable salt thereof, and an anti-inflammatory agent.

REFERENCES:
patent: WO 95/17204 (1995-06-01), None
patent: WO 00 01376 (2000-01-01), None
Smith et al., Jan. 2000, Nature Medicine, vol. 6, No. 1, pp. 62-66.
Guan et al., Mar. 2000, Brain Research, vol. 859, No. 2, pp. 286-292.
Smith, et al.: “Autoimmune encephalomyelitis ameliorated by AMPA antagonists”, Nature Medicine. U.S. Jan. 2000, vol. 6, No. 1. pp 62-66.
Guan, J., et al: “N-terminal tripeptide of IGF-1 (GPE) prevents the loss of TH positive neurons after 6-OHDA induced nigral lesion in rats.”, Brain Research, Netherlands Mar. 24, 2000, vol. 859, No. 2. pp. 286-292.
Kanwar, J.R., et al: “Beta7 integrins contribute to demyelinating disease of the central nervous system.”, Journal of Neuroimmunology. Netherlands Mar. 1, 2000, vol. 103, No. 2 pp. 146-152.

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