US2019240194A1PendingUtilityA1

Macrophages/microglia in neuro-inflammation associated with neurodegenerative diseases

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Assignee: MASSACHUSETTS GEN HOSPITALPriority: Aug 31, 2016Filed: Aug 31, 2017Published: Aug 8, 2019
Est. expiryAug 31, 2036(~10.1 yrs left)· nominal 20-yr term from priority
A61P 25/28A61K 9/0073C07D 311/24A61K 45/06A61K 9/0019C07D 311/22A61K 31/352A61K 31/7105A61K 31/428A61P 9/10A61P 25/14A61P 25/00
55
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Claims

Abstract

Described herein are methods of treating neuron inflammation conditions, for example, Alzheimer's disease, Parkinson's disease, Huntington's disease, ischemic stroke, and prion disease, comprising administering a therapeutically effective amount of cromolyn or a cromolyn derivative compound.

Claims

exact text as granted — not AI-modified
1 . A method of treating a neuron inflammation condition in a patient in need thereof comprising administering to the patient a therapeutically effective amount of at least one compound having the following formula: 
       
         
           
           
               
               
           
         
         provided the compound is not cromolyn disodium, 
       
       
         
           
           
               
               
           
         
         when the neuron inflammation condition is Alzheimer's Disease (AD). 
       
     
     
         2 . The method according to  claim 1 , wherein the compound has the following formula 
       
         
           
           
               
               
           
         
         
           
           
               
               
           
         
       
     
     
         3 . The method of  claim 1 , wherein the neuron inflammation condition is amyotrophic lateral scerlosis (ALS). 
     
     
         4 . The method of  claim 1 , wherein the neuron inflammation condition is AD. 
     
     
         5 . The method of  claim 1 , wherein the neuron inflammation is Huntington's Disease. 
     
     
         6 . The method of  claim 1 , wherein the neuron inflammation is Parkinson's disease (PD). 
     
     
         7 . The method of  claim 1 , wherein the neuron inflammation condition is ischemic stroke. 
     
     
         8 . The method of  claim 1 , wherein the neuron inflammation condition is associated with prion disease. 
     
     
         9 - 13 . (canceled) 
     
     
         14 . The method of  claim 3 , further comprising co-administering a second compound selected from CD4+; siRNA; miRNA that ameliorates ALS; glial morphology modifier; SOD1 control; and Riluzole. 
     
     
         15 . The method of  claim 3 , further comprising co-administering a second compound selected from an anti-aggregation drug and a targeting drug for AD. 
     
     
         16 . The method of  claim 1 , wherein the neuron inflammation condition is AD, further comprising co-administering a second compound selected from an antibody targeting drug that ameliorates AD. 
     
     
         17 . The method of  claim 1 , wherein the neuron inflammation condition is AD, further comprising co-administering a second compound selected from an anti-inflammatory targeting drug that ameliorates AD. 
     
     
         18 . The method of  claim 1 , wherein the neuron inflammation condition is AD, further comprising co-administering a second compound selected from a tau targeting drug that ameliorates AD. 
     
     
         19 . The method of  claim 3 , further comprising co-administering a second compound selected from an antibody targeting drug that ameliorates ALS. 
     
     
         20 . The method of  claim 3 , further comprising co-administering a second compound selected from an anti-inflammatory targeting drug that ameliorates ALS. 
     
     
         21 . The method of  claim 1 , further comprising co-administering a second compound selected from a targeting drug that ameliorates neurodegeneration associated with amyloidosis or tauopathies. 
     
     
         22 . The method of  claim 6 , further comprising co-administering a second compound selected from an alpha synuclein targeting drug that ameliorates PD and a Parkinson's targeting drug that ameliorates PD. 
     
     
         23 . The method of  claim 3 , wherein the compound is cromolyn disodium. 
     
     
         24 . The method of  claim 5 , wherein the compound is cromolyn disodium. 
     
     
         25 . The method of  claim 6 , wherein the compound is cromolyn disodium.

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