US2021093586A1PendingUtilityA1
Method of reducing neuronal cell death with haloalkylamines
Est. expirySep 6, 2033(~7.1 yrs left)· nominal 20-yr term from priority
A61K 9/0019A61P 11/00A61K 31/137A61P 9/10A61K 31/131A61P 25/28A61P 33/00A61P 27/02A61P 7/04A61P 43/00A61P 25/00A61K 31/138A61P 17/02A61P 33/14A61P 9/02
58
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The present invention is directed to pharmaceutical compositions and methods of treating traumatic brain injury (TBI). The invention is also directed to pharmaceutical compositions and methods of treating a transient hypoxic and/or ischemic condition in the central nervous system. More specifically, the present invention is directed to pharmaceutical compositions and methods of reducing the occurrence of nerounal cell death in the centeral nervous system, such as, reducing the occurrence brain cell death in the hippocampus and/or the cortex.
Claims
exact text as granted — not AI-modified1 - 39 . (canceled)
40 . A method of inhibiting neuronal cell death in a subject that is caused by a traumatic brain injury (TBI) event, the method comprising administering to the subject a pharmaceutical composition comprising phenoxybenzamine or a salt thereof in an amount sufficient to reduce neuronal cell death in the central nervous system of the subject.
41 . The method of claim 40 , further comprising determining that the subject has had a TBI event and is at risk of neuronal cell death, wherein the TBI event is selected from the group consisting of whiplash, a blast wave impact, and blunt force trauma.
42 . The method of claim 40 , wherein the pharmaceutical composition comprising phenoxybenzamine or salt thereof is administered in a single dose.
43 . The method according to claim 40 , wherein the phenoxybenzamine or salt thereof is in unit dosage amounts of about 0.5 mg/kg body weight to about 20 mg/kg body weight.
44 . The method according to claim 40 , wherein the pharmaceutical composition comprising phenoxybenzamine or salt thereof is administered with a pharmaceutically acceptable carrier.
45 . The method according to claim 40 , wherein the pharmaceutical composition comprising phenoxybenzamine or a salt thereof is in an extended release formulation.
46 . The method according to claim 41 , wherein the pharmaceutical composition comprising phenoxybenzamine or a salt thereof is administered within 24 hours after onset of the TBI event.
47 . The method according to claim 41 , wherein the pharmaceutical composition comprising phenoxybenzamine or a salt thereof is administered within 18 hours after onset of the TBI event.
48 . The method according to claim 41 , wherein the pharmaceutical composition comprising phenoxybenzamine or a salt thereof is administered in a single dose within 16 hours after onset of the TBI event.
49 . The method according to claim 40 , wherein the administering is via an intravenous injection.Join the waitlist — get patent alerts
Track US2021093586A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.