Neuromodulation device
US-2020009384-A1 · Jan 9, 2020 · US
US12239654B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12239654-B2 |
| Application number | US-201716095282-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 21, 2017 |
| Priority date | Apr 21, 2016 |
| Publication date | Mar 4, 2025 |
| Grant date | Mar 4, 2025 |
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The present invention relates to compounds and methods of use thereof for treatment of certain disorders and conditions, for example brain injuries such as stroke or traumatic brain injuries.
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We claim: 1. A method of treating an injury, disease, or condition selected from traumatic brain injury (TBI) and a stroke selected from ischemic stroke, hemorrhagic stroke, subarachnoid hemorrhage, cerebral vasospasm, and transient ischemic attacks (TIA), comprising administering to a patient in need thereof an effective amount of a compound selected from: or a pharmaceutically acceptable salt thereof. 2. The method of claim 1 , wherein the injury, disease, or condition is TBI. 3. The method of claim 2 , wherein the TBI is selected from concussion, blast injury, combat-related injury, or a mild, moderate or severe blow to the head. 4. The method of claim 1 , wherein the recovery period after the TBI or stroke is decreased as compared with an untreated patient. 5. The method of claim 1 , wherein the compound is administered chronically to treat stroke during the time period after the injury has occurred as it resolves. 6. The method of claim 1 , wherein the compound is selected from: or a pharmaceutically acceptable salt thereof. 7. The method of claim 1 , wherein the injury, disease, or condition is stroke and the compound or pharmaceutically acceptable salt thereof is administered within 48 hours of the stroke. 8. The method of claim 1 , wherein the injury, disease, or condition is stroke and the compound or pharmaceutically acceptable salt thereof is administered within 24 hours of the stroke. 9. The method of claim 1 , wherein the injury, disease, or condition is TBI and the compound or pharmaceutically acceptable salt thereof is administered within 48 hours of the TBI. 10. The method of claim 1 , wherein the injury, disease, or condition is TBI and the compound or pharmaceutically acceptable salt thereof is administered within 24 hours of the TBI. 11. The method of claim 2 , wherein neuroprotection or neurorestoration is increased in the patient as compared with an untreated patient.
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