Claims for Patent: 10,973,814

Summary for Patent: 10,973,814

Title:	Liquid naloxone spray
Abstract:	The invention provides stable liquid formulations containing naloxone, a pharmaceutically acceptable salt or a derivative thereof. The invention further provides methods for treating opioid overdose, opioid dependence, and congenital insensitivity to pain with anhidrosis by administering the liquid formulations of the present invention intranasally to a patient in need thereof. Further, the invention provides a method of treating opioid dependence, opioid overdose, and congenital insensitivity to pain with anhidrosis by administering intranasally the naloxone formulations of the present invention.
Inventor(s):	Amancha; Kiran (Chandler, AZ), Chilampalli; Chandeshwari (Chandler, AZ), Potta; Thrimoorthy (Phoenix, AZ), Yan; Ningxin (Chandler, AZ), Goskonda; Venkat R. (Phoenix, AZ)
Assignee:	HIKMA PHARMACEUTICALS USA INC. (Eatontown, NJ)
Application Number:	16/674,424
Patent Claims:	1. A liquid spray formulation comprising about 7.5% w/w naloxone, or a pharmaceutically acceptable salt thereof, about 66% w/w water, about 5.0% w/w propylene glycol, about 20.0% w/w ethanol and about 0.01% w/w edetate disodium dihydrate wherein the formulation does not contain an isotonicity agent or a buffer and wherein w/w denotes weight by weight of the total formulation. 2. A method of treating opioid dependence comprising administering the formulation of claim 1 to a patient in need thereof, wherein administration occurs either intranasally, sublingually or intranasally and sublingually, wherein if administration occurs intranasally and sublingually administration occurs simultaneously, sequentially or concomitantly. 3. A method of treating opioid overdose comprising administering the formulation of claim 1 to a patient in need thereof, wherein administration occurs either intranasally, sublingually or intranasally and sublingually, wherein if administration occurs intranasally and sublingually administration occurs simultaneously, sequentially or concomitantly. 4. A method of treating congenital insensitivity to pain with anhidrosis comprising administering the formulation of claim 1 to a patient in need thereof, wherein administration occurs either intranasally, sublingually or intranasally and sublingually, wherein if administration occurs intranasally and sublingually administration occurs simultaneously, sequentially or concomitantly. 5. A liquid spray formulation comprising about 9% w/w naloxone hydrochloride dihydrate, about 66% w/w water, about 5.0% w/w propylene glycol, about 20.0% w/w ethanol and about 0.01% w/w edetate disodium dihydrate wherein the formulation does not contain an isotonicity agent or a buffer and wherein w/w denotes weight by weight of the total formulation. 6. A method of treating opioid dependence comprising administering the formulation of claim 5 to a patient in need thereof, wherein administration occurs either intranasally, sublingually or intranasally and sublingually, wherein if administration occurs intranasally and sublingually administration occurs simultaneously, sequentially or concomitantly. 7. A method of treating opioid overdose comprising administering the formulation of claim 5 to a patient in need thereof, wherein administration occurs either intranasally, sublingually or intranasally and sublingually, wherein if administration occurs intranasally and sublingually administration occurs simultaneously, sequentially or concomitantly. 8. A method of treating congenital insensitivity to pain with anhidrosis comprising administering the formulation of claim 5 to a patient in need thereof, wherein administration occurs either intranasally, sublingually or intranasally and sublingually, wherein if administration occurs intranasally and sublingually administration occurs simultaneously, sequentially or concomitantly. 9. A liquid spray formulation comprising about 8% w/w naloxone hydrochloride, about 66% w/w water, about 5.0% w/w propylene glycol, about 20.0% w/w ethanol and about 0.01% w/w edetate disodium dihydrate wherein the formulation does not contain an isotonicity agent or a buffer and wherein w/w denotes weight by weight of the total formulation. 10. A method of treating opioid dependence comprising administering the formulation of claim 9 to a patient in need thereof, wherein administration occurs either intranasally, sublingually or intranasally and sublingually, wherein if administration occurs intranasally and sublingually administration occurs simultaneously, sequentially or concomitantly. 11. A method of treating opioid overdose comprising administering the formulation of claim 9 to a patient in need thereof, wherein administration occurs either intranasally, sublingually or intranasally and sublingually, wherein if administration occurs intranasally and sublingually administration occurs simultaneously, sequentially or concomitantly. 12. A method of treating congenital insensitivity to pain with anhidrosis comprising administering the formulation of claim 9 to a patient in need thereof, wherein administration occurs either intranasally, sublingually or intranasally and sublingually, wherein if administration occurs intranasally and sublingually administration occurs simultaneously, sequentially or concomitantly.