US2023077724A1PendingUtilityA1
Methods and compositions for treating cannabinoid overdose with a cannabinoid receptor antagonist
Assignee: OPIANT PHARMACEUTICALS INCPriority: Jun 18, 2019Filed: Oct 14, 2022Published: Mar 16, 2023
Est. expiryJun 18, 2039(~12.9 yrs left)· nominal 20-yr term from priority
Inventors:Phil Skolnick
C07D 205/04A61K 31/397A61K 9/0019
68
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Claims
Abstract
Disclosed herein are formulations and methods for reversing one or more symptoms of cannabinoid overdose, comprising parenterally administering a CB1 antagonist in an amount sufficient to reverse the cannabinoid overdose symptoms.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A composition formulated for parenteral administration comprising an amount of drinabant or a salt or polymorph thereof effective to reverse cannabinoid overdose or one or more symptoms thereof in a subject.
2 . The composition as recited in claim 1 , further comprising at least one agent that acts as a non-ionic solubilizer and/or emulsifying agent.
3 . A method of treating, reversing, or reducing cannabinoid overdose or one or more symptoms thereof in a subject, comprising parenterally administering to the subject an amount of drinabant or a salt or polymorph thereof, effective to treat, reverse, or reduce cannabinoid overdose or one or more symptoms thereof.
4 . The method as recited in claim 3 , wherein the plasma concentrations achieved by parenteral administration of drinabant or a salt or polymorph thereof sufficient to treat, reverse, or reduce cannabinoid overdose or one or more symptoms thereof is between about 200 ng/mL to about 730 ng/mL.
5 . The method as recited in claim 4 , wherein the parenteral route of administration is chosen from among intravenous (IV), intramuscular (IM), and subcutaneous (SC).
6 . The method as recited in claim 5 , wherein the parenteral route of administration is IV.
7 . The method as recited in claim 6 , wherein the IV dose is delivered by IV injection.
8 . The method as recited in claim 7 , wherein the IV dose is delivered in a liquid volume of between about 1 mL and about 20 mL.
9 . The method of claim 6 , wherein the IV dose is delivered by IV infusion.
10 . The method as recited in claim 9 , wherein the IV infusion is delivered in a liquid volume of between about 50 mL to about 500 mL.
11 . The method as recited in claim 9 , wherein the IV infusion is delivered over a period of about 30 minutes to about 2 hours.
12 . The method as recited in claim 9 , wherein the IV infusion is delivered at a rate of about 0.5 mL/minute to about 2 mL/minute.
13 . The method as recited in claim 9 , wherein the onset of reversal of symptom(s) of cannabinoid overdose is apparent within 30 minutes to about 60 minutes.
14 . The method as recited in claim 5 , wherein the parenteral route of administration is IM or SC.
15 . The method as recited in claim 14 , wherein the amount of drinabant, or a salt or polymorph thereof sufficient to reverse the cannabinoid overdose symptom(s) is between about 5 mg and about 100 mg per IM dose.
16 . The method as recited in claim 14 , wherein the SC dose is delivered in a liquid volume of between about 1 mL and about 1.5 mL.
17 . The method as recited in claim 3 , wherein if no response is observed within about 30 minutes to about 2 hours of a first administration of drinabant, and the presence of cannabinoids is confirmed or strongly suspected, a second dose may be administered.Join the waitlist — get patent alerts
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