US2019175542A1PendingUtilityA1

Methods of treating age related disorders

Assignee: ZAFGEN INCPriority: Oct 3, 2011Filed: Jun 27, 2018Published: Jun 13, 2019
Est. expiryOct 3, 2031(~5.2 yrs left)· nominal 20-yr term from priority
A61P 39/06A61P 39/00A61P 9/00A61P 3/04A61P 25/24A61P 25/28A61P 21/00A61K 31/7088A61K 31/335C07D 303/08A61P 19/00A61K 9/0053C07D 303/18A61K 31/713A61K 9/0019A61P 19/02C07D 303/12A61P 25/00A61K 31/336
57
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

The invention generally relates to methods of treating a patient having, and/or at risk of, oxidative distress disorders and/or age-related disorders. The disclosure also generally relates to methods of treating memory impairment or enhancing the cognitive function of a patient in need thereof. Such methods may include administering a therapeutically effective amount of a MetAP2 inhibitor.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of treating an age-related neuromuscular disorder in a patient in need thereof, comprising administering to the patient an effective amount of an irreversible MetAP2 inhibitor that covalently binds to MetAP2, wherein said inhibitor, upon administration increases the level of metabolic products formed in the citric acid cycle and does not substantially increase alphaketoglutarate in the liver of said patient. 
     
     
         2 . The method of  claim 1 , wherein said patient exhibits a reduction in expression of mCLK1. 
     
     
         3 . The method of  claim 1 , wherein the patient, upon administration of the MetAP2 inhibitor, exhibits a decrease in non-mitochondrial oxidative damage. 
     
     
         4 . The method of  claim 1 , wherein the patient, upon administration of the MetAP2 inhibitor, exhibits increased mitochondrial oxidative stress. 
     
     
         5 . The method of  claim 1 , wherein said therapeutically effective amount does not substantially modulate or suppress angiogenesis. 
     
     
         6 . The method of  claim 1 , further comprising administration of the MetAP2 inhibitor until a marker level is returned to a normal range. 
     
     
         7 . The method of  claim 6 , wherein the marker is C-reactive protein. 
     
     
         8 . The method of  claim 1 , wherein said MetAP2 inhibitor is administered parenterally or non-parenterally. 
     
     
         9 . The method of  claim 1 , wherein the MetAP2 inhibitor is a fumagillin analog. 
     
     
         10 . The method of  claim 9 , wherein the MetAP2 inhibitor is administered at a dose of about 0.01 mg/kg to about 10 mg/kg. 
     
     
         11 . The method of  claim 9 , wherein the MetAP2 inhibitor is administered at a dose of about 0.04 mg/kg to about 1.0 mg/kg. 
     
     
         12 . The method of  claim 1 , wherein the age-related neuromuscular disorder is sarcopenia. 
     
     
         13 . A method of treating sarcopenia in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of an irreversible MetAP2 inhibitor that covalently binds to MetAP2, wherein the therapeutically effective amount does not substantially modulate or suppress angiogenesis.

Join the waitlist — get patent alerts

Track US2019175542A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.