METHODS AND PRODUCTS FOR TREATMENT OF DISEASES
The invention provides a method of treating a disease or condition mediated by vascular hyperpermeability in an animal. The method comprises administering an amount of a danazol compound effective to inhibit vascular hyperpermeability and an amount of a second drug effective to treat the disease or condition. The invention further provides a method of inhibiting vascular hyperpermeability when it is a side effect caused by administration of a drug to, or another treatment of, an animal. The method comprises administration of an amount of a danazol compound effective to inhibit the vascular hyperpermeability. The invention also provides a method of modulating the cytoskeleton of endothelial cells in an animal comprising administering an amount of a danazol compound and an amount of a second drug effective to modulate the cytoskeleton. The present invention also relates to pharmaceutical compositions and kits comprising a danazol compound and a second drug.
1 - 34 . (canceled)
35 . A pharmaceutical composition comprising a pharmaceutically-acceptable carrier, a first drug and a second drug, wherein the first drug is a danazol compound and the second drug is a drug suitable for treating a disease or condition mediated by vascular hyperpermeability.
36 . The composition of claim 35 wherein the second drug is one that inhibits vascular hyperpermeability.
37 . The composition of claim 35 wherein the second drug is one that inhibits vascular endothelial growth factor.
38 . The composition of claim 35 wherein the second drug is an antihistamine.
39 . The composition of claim 35 wherein the second drug is a drug that lowers the level of glucose.
40 . The composition of claim 35 wherein the second drug is an angiotensin converting enzyme (ACE) inhibitor or an ACE receptor antagonist.
41 . The composition of claim 35 wherein the second drug is an anti-inflammatory drug.
42 . The composition of claim 35 wherein the second drug is an antioxidant.
43 . The composition of claim 35 wherein the second drug is a statin.
44 . The composition of claim 35 wherein the second drug is sphingosine-1 phosphate (S1P) or a S1P agonist.
45 . The composition of claim 35 wherein the second drug is an inhibitor of an enzyme that degrades a glycocalyx.
46 . A kit comprising a first container and a second container, wherein the first container comprises a danazol compound and the second container comprises a drug suitable for treating a disease or condition mediated by vascular hyperpermeability.
47 . The kit of claim 46 wherein the drug in the second container is one that inhibits vascular hyperpermeability.
48 . The kit of claim 46 wherein the drug in the second container is one that inhibits vascular endothelial growth factor.
49 . The kit of claim 46 wherein the drug in the second container is an antihistamine.
50 . The kit of claim 46 wherein the drug in the second container is a drug that lowers the level of glucose.
51 . The kit of claim 46 wherein the drug in the second container is an angiotensin converting enzyme (ACE) inhibitor or an ACE receptor antagonist.
52 . The kit of claim 46 wherein the drug in the second container is an anti-inflammatory drug.
53 . The kit of claim 46 wherein the drug in the second container is an antioxidant.
54 . The kit of claim 46 wherein the drug in the second container is a statin.
55 . The kit of claim 46 wherein the drug in the second container is sphingosine-1 phosphate (S1P) or a S1P agonist.
56 . The kit of claim 46 wherein the drug in the second container is an inhibitor of an enzyme that degrades a glycocalyx.
57 .- 62 . (canceled)
63 . A pharmaceutical composition comprising a pharmaceutically-acceptable carrier, a first drug and a second drug, wherein the first drug is danazol or a pharmaceutically-acceptable salt thereof and the second drug is a drug selected from the group consisting of a drug that inhibits vascular hyperpermeability, a drug that inhibits vascular endothelial growth factor, a drug that is an antihistamine, a drug that inhibits angiogenesis, a drug that is a protein kinase C inhibitor, a drug that is an anti-inflammatory drug, a drug that is sphingosine-1 phosphate (S1P) or a S1P agonist, a drug that is an inhibitor of an enzyme that degrades a glycocalyx, a drug that lowers the level of glucose, a drug that is an antioxidant, a drug that is a statin, and a drug that is an angiotensin converting enzyme (ACE) inhibitor or an ACE receptor antagonist.
64 . The composition of claim 63 wherein the second drug is one that inhibits vascular hyperpermeability.
65 . The composition of claim 63 wherein the second drug is one that inhibits vascular endothelial growth factor.
66 . The composition of claim 63 wherein the second drug is an antihistamine.
67 . The composition of claim 63 wherein the second drug is a drug that lowers the level of glucose.
68 . The composition of claim 63 wherein the second drug is an angiotensin converting enzyme (ACE) inhibitor or an ACE receptor antagonist.
69 . The composition of claim 63 wherein the second drug is an anti-inflammatory drug.
70 . The composition of claim 63 wherein the second drug is an antioxidant.