Claims for Patent: 11,975,096

Summary for Patent: 11,975,096

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):	Kiran Amancha, Chandeshwari Chilampalli, Thrimoorthy Potta, Ningxin Yan, Venkat R. Goskonda
Assignee:	Hikma Pharmaceuticals USA Inc
Application Number:	US17/411,507
Patent Claims:	1. A nasal spray formulation comprising from about 5% to about 15% w/w naloxone or a pharmaceutically acceptable salt thereof, from about 0.001% to about 0.5% w/w of a chelating agent, ethanol, propylene glycol, and water, wherein w/w denotes weight by total weight of the formulation. 2. The formulation of claim 1, wherein the chelating agent is edetate disodium dihydrate. 3. The formulation of claim 1, wherein the ethanol is at a concentration from about 20% to about 50% w/w and the propylene glycol is at a concentration from about 5% to about 10% w/w. 4. The formulation of claim 1, further comprising from about 0.001% to about 0.2% w/w of a permeation enhancer. 5. The formulation of claim 4, wherein the permeation enhancer is benzalkonium chloride. 6. The formulation of claim 1, further comprising one or more pH adjustors. 7. The formulation of claim 1, wherein the pH is from about 3 to about 6. 8. The formulation of claim 1, wherein the pH is from about 4 to about 5. 9. The formulation of claim 1, wherein the naloxone or pharmaceutically acceptable salt thereof, is at a concentration of about 8% w/w. 10. The formulation of claim 1, wherein the water is at a concentration from about 20% to about 95% w/w. 11. A nasal spray formulation comprising from about 5% to about 10% w/w naloxone or a pharmaceutically acceptable salt thereof, from about 0.001% to about 0.5% w/w of a chelating agent, from about 0.005% to about 0.10% w/w of a permeation enhancer, ethanol, propylene glycol, and water, wherein w/w denotes weight by total weight of the formulation. 12. The formulation of claim 11, wherein the permeation enhancer is at a concentration from about 0.01% to about 0.1% w/w. 13. The formulation of claim 11, wherein the chelating agent is edetate disodium dihydrate. 14. The formulation of claim 11, wherein the permeation enhancer is benzalkonium chloride. 15. The formulation of claim 14, wherein the benzalkonium chloride is at a concentration of about 0.01% w/w. 16. The formulation of claim 11, wherein the naloxone or pharmaceutically acceptable salt thereof, is at a concentration of about 8% w/w. 17. The formulation of claim 11, further comprising one or more pH adjustors. 18. The formulation of claim 11, wherein the pH is from about 3 to about 6. 19. The formulation of claim 11, wherein the pH is from about 4 to about 5.