US2013266578A1PendingUtilityA1
Methods of treating an overweight subject
Est. expiryApr 7, 2030(~3.7 yrs left)· nominal 20-yr term from priority
C12N 2310/14C12N 2310/11A61K 45/06A61K 31/4025C12N 2310/531A61K 31/196C12N 15/1137A61K 31/336C12Y 304/11018A61K 31/439
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Claims
Abstract
The invention generally relates in part to methods of effecting weight loss and/or improving glucose tolerance in a patient in need thereof, comprising administering a MetAP2 inhibitor.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of effecting weight loss in a patient in need thereof, comprising administering a pharmaceutically effective amount of a MetAP2 inhibitor to the patient, wherein upon discontinuation of administration of said MetAP2 inhibitor, the patient has durable weight loss maintained at least for about 1 month.
2 . The method of claim 1 , wherein the durable weight loss is maintained for at least about 3 months.
3 . The method of claim 1 , wherein the patient is overweight or obese.
4 . A method of inhibiting further weight gain in an overweight or obese patient, comprising administering a pharmaceutically effective amount of a MetAP2 inhibitor to the patient.
5 . The method of claim 4 , wherein the patient is overweight.
6 . The method of claim 5 , wherein the patient is not obese.
7 . A method of increasing and/or improving glucose tolerance and /or glycemic control in a patient in need thereof, comprising administering a pharmaceutically effective amount of a MetAP2 inhibitor to the patient.
8 . The method of claim 7 , wherein the patient is suffering from type 2 diabetes.
9 . The method of claim 7 , wherein the patient has impaired glucose tolerance and/or impaired fasting glucose.
10 . The method of claim 1 , wherein said MetAP2 inhibitor is administered alone or in combination with another active agent.
11 . The method of claim 1 , wherein said MetAP2 inhibitor is administered buccally, sublingually or transdermally.
12 . The method of claim 1 , wherein said MetAP2 inhibitor is administered subcutaneously or intravenously.
13 . The method of claim 1 , wherein said MetAP2 inhibitor is administered via inhalation.
14 . The method of claim 1 , wherein said MetAP2 inhibitor is administered rectally.
15 . The method of claim 1 , wherein said MetAP2 inhibitor is a substantially irreversible inhibitor.
16 . The method of claim 1 , wherein said MetAP2 inhibitor is selected from the group consisting of a fumagillin, fumagillol or fumagillin ketone derivative, siRNA, shRNA, an antibody, or a antisense compound.
17 . The method of claim 1 , wherein said MetAP2 inhibitor is selected from O-(4-dimethylaminoethoxycinnamoyl)fumagillol and pharmaceutically acceptable salts thereof
18 . The method of claim 1 , wherein said non-parenterally administering results in decreased body fat and a substantial maintenance of muscle mass in said patient.
19 . The method of claim 1 , wherein upon administration, fat oxidation is enhanced as compared to a patient on a restricted food intake diet alone.
20 . A method for reducing the amount or frequency of administering supplemental insulin in a patient suffering from type 2 diabetes, comprising a pharmaceutically effective amount of a MetAP2 inhibitor.
21 . A method of maintaining a specified weight in a formerly obese patient, comprising administering a pharmaceutically effective amount of a MetAP2 inhibitor to said patient.
22 . The method of claim 21 , wherein the pharmaceutically effective amount is less as compared to the amount needed to reduce weight or body fat.
23 . The method of claim 20 , wherein said pharmaceutically effective amount does not substantially modulate or suppress angiogenesis.
24 . The method of claim 20 , wherein said MetAP2 inhibitor is a substantially irreversible inhibitor.
25 . The method of claim 20 , wherein said MetAP2 inhibitor is selected from the group consisting of a fumagillin, fumagillol or fumagillin ketone derivative, siRNA, shRNA, an antibody, or an antisense compound.
26 . The method of claim 20 , wherein said MetAP2 inhibitor is selected from O-(4-dimethylaminoethoxycinnamoyl)fumagillol and pharmaceutically acceptable salts thereof.
27 . The method of claim 1 , further comprising co-administering an additional weight loss agent.
28 . The method of claim 1 , further comprising administering a food restricted diet to said patient.
29 . The method of claim 1 , wherein said administration occurs at least daily.
30 . The method of claim 1 , wherein said administration occurs at least weekly.Cited by (0)
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