Urat1 inhibitor, pharmaceutical compositions and uses thereof
US-2024226070-A1 · Jul 11, 2024 · US
US10220077B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10220077-B2 |
| Application number | US-201314442731-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 14, 2013 |
| Priority date | Nov 14, 2012 |
| Publication date | Mar 5, 2019 |
| Grant date | Mar 5, 2019 |
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A method of treating a disease selected from the group consisting of emphysema, sepsis, septic shock, ischemic injury, cerebral ischemia, a neurodegenerative disorder, meningitis, encephalitis, hemorrhage, cerebral ischemia, heart ischemia and a cognitive deficit in a subject in need thereof is provided. The method comprising administering to the subject a therapeutically effective amount of a combination of at least two agents, wherein a first of said two agents upregulates an activity and/or expression of Nrf2 and a second of said two agents is a glutamatergic modulator, thereby treating the disease.
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What is claimed is: 1. A method of treating a disease selected from the group consisting of ischemic injury, cerebral ischemia, and a neurodegenerative disorder selected from the group consisting of amyotrophic lateral sclerosis, and multiple system atrophy, in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a combination of three agents, wherein a first of said three agents is a polynucleotide encoding Nuclear factor (erythroid-derived 2)-like 2 (Nrf2), a second of said three agents is a polynucleotide encoding a glutamate transporter and a third of said three agents is a polynucleotide encoding a glutamate dehydrogenase, thereby treating the disease, and wherein the glutamate transporter is excitatory amino acid transporter (EAAT) 2 (EAAT2) and the glutamate dehydrogenase is glutamate dehydrogenase 2 (GDH2). 2. The method of claim 1 , wherein the neurodegenerative disorder is amyotrophic lateral sclerosis or multiple system atrophy. 3. The method of claim 1 , further comprising administering an antioxidant. 4. The method of claim 3 , wherein said antioxidant comprises an agent selected from the group consisting of Coenzyme Q10, thiol, ascorbic acid, polyphenol, glutathione, vitamin C, vitamin E, catalase, superoxide dismutase and peroxidase. 5. The method of claim 1 , wherein said administering is effected via intra-cisternal (I.C.) administration or intra-muscular (I.M.) administration. 6. The method of claim 1 , wherein said disease is ischemic injury or cerebral ischemia.
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