US2006013808A1PendingUtilityA1
Treatment for asthma
Assignee: BIOGEN INC A MASSACHUSETTS CORPriority: Jan 13, 1992Filed: Jun 28, 2005Published: Jan 19, 2006
Est. expiryJan 13, 2012(expired)· nominal 20-yr term from priority
C07K 2319/30C07K 14/78C07K 16/2842A61K 2039/505A61K 38/00C07K 2319/00C07K 14/70542
51
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Claims
Abstract
A method for the treatment of asthma is disclosed. The method comprises administration of an antibody, polypeptide or other molecule recognizing VLA-4, a protein expressed on the surface of certain leukocytes such as eosinophils.
Claims
exact text as granted — not AI-modified1 - 25 . (canceled)
26 . A method for the treatment of asthma comprising administering to a mammal suffering from asthma a composition comprising a chimeric molecule comprising a fibronectin polypeptide and a toxin moiety.
27 . The method of claim 26 , wherein the toxin moiety is selected from the group consisting of Diphtheria toxin A, Pseudomonas Exotoxin, Ricin A, Abrin A, Schigella toxin, and Gelonin.
28 . The method of claim 26 , wherein the toxin moiety is selected from the group consisting of a radionucleotide and a chemotherapeutic agent.
29 . The method of claim 26 , wherein the composition is administered intravenously.
30 . The method of claim 26 , wherein the composition is administered in the form of an aerosol by inhalation.
31 . The method of claim 26 , wherein the composition is administered at a dosage so as to provide from 0.05 to 5.0 mg/kg of the chimeric molecule, based on the weight of the mammal.
32 . The method of claim 31 , wherein the composition is administered to the mammal at a dosage so as to provide 0.5 to 2.0 mg/kg of chimeric molecule, based on the weight of the mammal.
33 . The method of claim 26 , wherein the composition is administered to the mammal prior to exposure to an allergen to which the mammal is hypersensitive.
34 . The method of claim 26 , wherein the composition is administered to the mammal after exposure to an allergen to which the mammal is hypersensitive.
35 . The method of claim 26 , wherein the mammal is a human.
36 . The method of claim 26 , wherein the fibronectin polypeptide comprises an EILDV motif (SEQ ID NO:16).
37 . The method of claim 26 , wherein the fibronectin polypeptide comprises an alternatively spliced non-type III connecting segment.
38 . A chimeric molecule comprising a fibronectin polypeptide and a toxin moiety.
39 . The chimeric molecule of claim 38 , wherein the toxin moiety is selected from the group consisting of Diphtheria toxin A, Pseudomonas Exotoxin, Ricin A, Abrin A, Schigella toxin, and Gelonin.
40 . The chimeric molecule of claim 38 , wherein the toxin moiety is selected from the group consisting of a radionucleotide and a chemotherapeutic agent.
41 . The chimeric molecule of claim 38 , wherein the fibronectin polypeptide comprises an EILDV motif (SEQ ID NO:16).
42 . The chimeric molecule of claim 38 , wherein the fibronectin polypeptide comprises an alternatively spliced non-type III connecting segment.Join the waitlist — get patent alerts
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