Details for Patent: 9,561,177

Title:	Nasal drug products and methods of their use
Abstract:	Drug products adapted for nasal delivery, comprising a pre-primed device filled with a pharmaceutical composition comprising an opioid receptor antagonist, are provided. Methods of treating opioid overdose or its symptoms with the inventive drug products are also provided.
Inventor(s):	Keegan; Fintan (Dublin, IE), Bell; Robert Gerard (Clearwater, FL), Crystal; Roger (Santa Monica, CA), Weiss; Michael Brenner (New York, NY)
Assignee:	ADAPT PHARMA LIMITED (Dublin, IE) OPIANT PHARMACEUTICALS (Santa Monica, CA)
Filing Date:	Jun 15, 2016
Application Number:	15/183,441
Claims:	1. A method of treating opioid overdose, the method comprising: delivering a 25-200 .mu.L spray of a pharmaceutical solution from a pre-primed device into a nostril of a patient, wherein the device is adapted for nasal delivery, and wherein the pharmaceutical solution comprises about 4 mg naloxone hydrochloride or a hydrate thereof, between about 0.005% and about 0.015% (w/v) of benzalkonium chloride, and an isotonicity agent. 2. The method of claim 1, wherein the pharmaceutical solution comprises between about 0.2% and about 1.2% (w/v) of the isotonicity agent. 3. The method of claim 2, wherein the pharmaceutical solution further comprises between about 0.1% and about 0.5% (w/v) of a stabilizing agent and an amount of an acid sufficient to achieve a pH between about 3.5 and about 5.5. 4. The method of claim 3, wherein: the isotonicity agent is sodium chloride; the stabilizing agent is disodium edetate; and the acid is hydrochloric acid. 5. The method of claim 4, wherein the pharmaceutical solution comprises: about 4% (w/v) naloxone hydrochloride; about 0.74% (w/v) sodium chloride; about 0.01% (w/v) benzalkonium chloride; and about 0.2% (w/v) disodium edetate. 6. The method of claim 5, wherein the device has a single reservoir containing approximately 125 .mu.L of the pharmaceutical solution. 7. The method of claim 6, wherein approximately 100 .mu.L of the pharmaceutical solution is delivered by one actuation of the device. 8. The method of claim 7, wherein the device comprises a reservoir, a piston, and a swirl chamber. 9. The method of claim 6, further comprising storing the device for about twelve months or less at 25.degree. C. and 60% relative humidity prior to actuating the device, wherein the device retains at least about 100% of initial naloxone hydrochloride content at actuation. 10. The method of claim 1, wherein the patient experiences a geometric mean naloxone C.sub.max not less than about 3 ng/mL following a single spray. 11. The method of claim 10, wherein the patient experiences a plasma naloxone concentration such that the geometric mean of area under a plasma concentration versus time curve (AUC.sub.0-.infin.) is not less than about 8 hr*ng/mL when time is extrapolated to infinity. 12. A mist delivered from a pre-primed device, wherein the mist comprises droplets, wherein the droplets comprise, in aggregate, about 4 mg of naloxone hydrochloride or a hydrate thereof, between about 0.005% and about 1% (w/v) of benzalkonium chloride, and an isotonicity agent, wherein no more than about 10% of the droplets have a diameter less than 10 .mu.m. 13. The mist of claim 12, wherein the mist comprises the isotonicity agent in a concentration between about 0.2% and about 1.2% (w/v). 14. The mist of claim 13, wherein the isotonicity agent is sodium chloride. 15. The mist of claim 12, wherein the mist takes the shape of a round plume with an ovality ratio less than 2.0. 16. The mist of claim 12, wherein the naloxone is at least 40% bioavailable. 17. The mist of claim 16, wherein the median droplet size is between about 30 .mu.m and about 100 .mu.m. 18. The mist of claim 17, wherein approximately 50% of droplets have a diameter between about 30 .mu.m and about 70 .mu.m. 19. The mist of claim 18, wherein approximately 90% of droplets have a diameter less than about 100 .mu.m. 20. The mist of claim 19, wherein no more than approximately 2% of droplets have a diameter less than about 10 .mu.m. 21. The mist of claim 12, wherein the mist stands adjacent to an aperture in a single-dose spray device or a bi-dose spray device. 22. A method of treating narcotic-induced respiratory depression, the method comprising: delivering a 25-200 .mu.L spray of a pharmaceutical solution from a pre-primed device into a nostril of a patient in need thereof in a manner that delivers the pharmaceutical solution in a round spray plume with an ovality ratio less than about 2.0 when measured at 3 cm, wherein the device is adapted for nasal delivery, and wherein the spray comprises about 4 mg naloxone hydrochloride or a hydrate thereof, between about 0.005% and about 0.015% (w/y) ref benzaikonium chloride, and an isotonicity agent wherein the patient experiences a geometric mean naloxone C.sub.max not less than about 3 ng/ml, following a single spray. 23. The method of claim 22, wherein the pharmaceutical solution comprises between about 0.2% and about 1.2% (w/v) of the isotonicity agent. 24. The method of claim 23, wherein the pharmaceutical solution further comprises between about 0.1% and about 0.5% (w/v) of a stabilizing agent. 25. The method of claim 24, wherein the pharmaceutical solution further comprises an amount of an acid sufficient to achieve a pH between about 3.5 and about 5.5. 26. The method of claim 25, wherein: the isotonicity agent is sodium chloride; the stabilizing agent is disodium edetate; and the acid is hydrochloric acid. 27. The method of claim 26, wherein the acid is hydrochloric acid and wherein the pharmaceutical solution comprises: about 4% (w/v) naloxone hydrochloride; about 0.74% (w/v) sodium chloride as the isotonicity agent; about 0.01% (w/v) benzalkonium chloride; and about 0.2% (w/v) disodium edetate as the stabilizing agent. 28. The method of claim 22, wherein the plasma concentration versus time curve of naloxone in the patient has a t.sub.max of less than 30 minutes. 29. The method of claim 22, wherein the ovality ratio is less than about 1.5when measured at 3 cm. 30. The method of claim 22, wherein the device comprises a plunger that houses a container closure comprising a vial comprising an opening, a cannula, and a rubber stopper, wherein the stopper is configured to occlude the opening of the vial, and wherein the cannula is configured such that the cannula can pierce the stopper when the plunger applies sufficient force to the cannula.