Therapeutic chemokine receptor antagonists

A - Human Necessities – 61 – K

Patent

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Details

A61K 38/21 (2006.01) A61K 38/17 (2006.01) C07K 14/52 (2006.01) C07K 14/715 (2006.01) A61K 38/00 (2006.01)

Patent

CA 2322764

The invention provides a variety of therapeutic uses for CXCR4 antagonists. In various embodiments, CXCR4 antagonists may be used as therapeutically as follows, or to manufacture a medicament for such therapeutic treatments: reducing interferon gamma production by T-cells, treatment of an autoimmune disease, treatment multiple sclerosis, treatment of cancer, inhibition of angiogenesis. The invention provides corresponding methods of medical treatment, in which a therapeutic dose of a CXCR4 antagonist is administered in a pharmacologically acceptable formulation. Accordingly, the invention also provides therapeutic compositions comprising a CXCR4 antagonist and a pharmacologically acceptable excipient or carrier. The CXCR4 antagonists for use in the invention may be peptide compounds comprising a substantially purified peptide fragment, modified fragment, analogue or pharmacologically acceptable salt of SDF-1.

La présente invention concerne diverses utilisations thérapeutiques des antagonistes de CXCR4. Dans des réalisations diverses, des antagonistes de CXCR4 sont utilisés pour la fabrication de médicaments ou sont utilisés dans les traitements tels que la réduction de la production d'interféron gamma par les cellules T, le traitement d'une maladie auto-immune, le traitement de la sclérose multiple, le traitement du cancer, et l'inhibition de l'angiogénèse. La présente invention concerne aussi les procédés des traitements associés dans lesquels une dose d'un antagoniste de CXCR4 est administrée à l'aide d'une formulation d'usage pharmacologique. Cette invention concerne donc aussi des compositions thérapeutiques qui comprennent un antagoniste de CXCR4 et un excipient ou un support d'usage pharmacologique. Les antagonistes de CXCR4 de l'invention sont des composés de type peptide qui comprennent un fragment peptide sensiblement purifié, un fragment modifié, un analogue ou un sel de SDF-1 acceptable sur le plan pharmacologique.

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