Claims for Patent: 12,514,854

Summary for Patent: 12,514,854

Title:	Drug products for intranasal administration and uses thereof
Abstract:	Provided herein are methods of using drug products adapted for nasal delivery comprising a device and a pharmaceutical composition comprising an opioid receptor antagonist, wherein the claimed invention provides a method of treating an opioid overdose or symptom thereof in a patient in need thereof, comprising intranasally administering to the patient an aqueous pharmaceutical solution consisting of, or an aqueous pharmaceutical composition consisting essentially of: (i) naloxone hydrochloride in an amount of about 9% by weight based on the total weight of the aqueous pharmaceutical solution; (ii) glycerin in an amount of about 1.4% by weight based on the total weight of the aqueous pharmaceutical solution; (iii) a citrate buffer system adjusted by hydrochloric acid and/or sodium hydroxide; and (iv) United States Pharmacopeia (USP)—grade Purified Water; wherein the pH of the aqueous pharmaceutical solution is from about 3.5 to about 4.7; and wherein the hydrochloric acid and the sodium hydroxide may each be independently present in the aqueous pharmaceutical solution, as required, to achieve the pH from about 3.5 to about 4.7.
Inventor(s):	Gregory G. Plucinski, Adrian T. Raiche, Kristi R. Sims
Assignee:	Summit Biosciences Inc
Application Number:	US18/602,984
Patent Claims:	1. A method of treating an opioid overdose or symptom thereof in a patient in need thereof, comprising: (a) providing a unit dose of an aqueous pharmaceutical solution housed in a device configured for intranasal administration of the unit dose, wherein the aqueous pharmaceutical solution consists of: (i) naloxone hydrochloride in an amount of about 9% by weight based on the total weight of the aqueous pharmaceutical solution; (ii) glycerin in an amount of about 1.4% by weight based on the total weight of the aqueous pharmaceutical solution; (iii) a citrate buffer system adjusted by hydrochloric acid and/or sodium hydroxide; and (iv) United States Pharmacopeia (USP)-grade Purified Water; wherein the pH of the aqueous pharmaceutical solution is from about 3.5 to about 4.7; wherein the hydrochloric acid and the sodium hydroxide may each be independently present in the aqueous pharmaceutical solution, as required, to achieve the pH from about 3.5 to about 4.7; and wherein the osmolality of the aqueous pharmaceutical solution is about 560 mOsm/kg; and (b) intranasally administering the unit dose to the patient, wherein intranasally administering comprises performing a single actuation of the device to deliver the unit dose to the patient; and wherein the method does not comprise priming the device prior to intranasally administering the unit dose to the patient. 2. The method of claim 1, wherein the pH of the solution is about 4.3. 3. The method of claim 1, wherein the citrate buffer is in an amount of about 0.2% to about 0.4% by weight based on the total weight of the aqueous pharmaceutical solution. 4. The method of claim 1, wherein the patient is a human patient. 5. The method of claim 4, wherein the human patient is an adult. 6. The method of claim 4, wherein the human patient is a pediatric patient.