COMPOSITIONS AND METHODS FOR THE TREATMENT OF OPIOID OVERDOSE
Drug products adapted for nasal delivery, comprising a pre-primed device filled with a pharmaceutical composition comprising nalmefene are provided. Methods of treating opioid overdose with the drug products are also provided.
1 - 71 . (canceled)
72 . A pharmaceutical formulation for intranasal administration comprising:
(a) from about 1% (w/v) to about 4% (w/v) of nalmefene or a pharmaceutically acceptable salt or solvate thereof;
(b) from about 0.1% (w/v) to about 2.5% (w/v) dodecyl maltoside;
(c) from about 0.2% (w/v) to about 1.2% (w/v) of sodium chloride;
(d) from about 0.005% (w/v) to about 1% (w/v) of a preservative;
(e) from about 0.1% (w/v) to about 0.5% (w/v) of disodium edetate; and
(f) water in an amount sufficient to achieve a final volume of about 50 to about 250 microliters.
73 . The pharmaceutical formulation of claim 72 , comprising about 3% (w/v) of nalmefene hydrochloride.
74 . The pharmaceutical formulation of claim 72 , comprising about 2.7% (w/v) of nalmefene free base.
75 . The pharmaceutical formulation of claim 72 , comprising about 0.25% (w/v) of dodecyl maltoside.
76 . The pharmaceutical formulation of claim 72 , wherein the preservative comprises benzalkonium chloride.
77 . The pharmaceutical formulation of claim 76 , comprising about 0.04% (w/v) of benzalkonium chloride.
78 . The pharmaceutical formulation of claim 72 , comprising about 0.87% (w/v) of sodium chloride.
79 . The pharmaceutical formulation of claim 72 , comprising about 0.2% (w/v) of disodium edetate.
80 . The pharmaceutical formulation of claim 72 , further comprising an acid.
81 . The pharmaceutical formulation of claim 80 , wherein the acid comprises hydrochloric acid.
82 . The pharmaceutical formulation of claim 72 , wherein the pH of the formulation ranges from about 3.5 to about 5.5.
83 . A method of treating opioid overdose or a symptom thereof in a human, the method comprising administering from about 50 to 250 microliters of the pharmaceutical formulation of claim 72 to said human.
84 . The method of claim 83 , wherein the symptom is chosen from respiratory depression, central nervous system depression, altered level consciousness, miotic pupils, cardiovascular depression, hypoxemia, acute lung injury, aspiration pneumonia, sedation, unresponsiveness to stimulus, unconsciousness, stopped breathing, erratic or stopped pulse, choking or gurgling sounds, blue or purple fingernails or lips, slack or limp muscle tone, contracted pupils, vomiting, and hypotension.
85 . A pharmaceutical formulation for intranasal administration, comprising:
(a) from about 1 mg to about 4 mg of nalmefene or a pharmaceutically acceptable salt thereof;
(b) from about 0.1 mg to about 2.5 mg of dodecyl maltoside;
(c) from about 0.2 mg to about 1.2 mg of sodium chloride;
(d) from about 0.005 mg to about 1 mg of a preservative;
(e) from about 0.1 mg to about 0.5 mg of disodium edetate; and
(f) water in an amount sufficient to achieve a final volume of about 50 to about 250 microliters.
86 . The pharmaceutical formulation of claim 85 , wherein the nalmefene comprises about 3 mg of nalmefene hydrochloride.
87 . The pharmaceutical formulation of claim 85 , wherein the nalmefene comprises about 2.7 mg of nalmefene free base.
88 . The pharmaceutical formulation of claim 85 , comprising about 0.25 mg of dodecyl maltoside.
89 . The pharmaceutical formulation of claim 85 , wherein the preservative is benzalkonium chloride.
90 . The pharmaceutical formulation of claim 89 , comprising about 0.04 mg of benzalkonium chloride.
91 . The pharmaceutical formulation of claim 85 , comprising about 0.87 mg of sodium chloride.
92 . The pharmaceutical formulation of claim 85 , comprising about 0.2 mg of disodium edetate.
93 . The pharmaceutical formulation of claim 85 , further comprising an acid.
94 . The pharmaceutical formulation of claim 93 , wherein the acid is hydrochloric acid.
95 . A method of treating opioid overdose or a symptom thereof in a human, the method comprising administering a therapeutically effective amount of the pharmaceutical formulation of claim 85 to said human.
96 . The method of claim 95 , wherein the opioid overdose is caused by a synthetic opioid.
97 . The method of claim 95 , wherein the opioid overdose is caused by fentanyl or a derivative thereof.
98 . The method of claim 95 , wherein the pharmaceutical formulation is administered to said human by a single-use, pre-primed device adapted for nasal delivery of the therapeutically effective amount of the pharmaceutical formulation to said human.
99 . The method of claim 98 , wherein the pharmaceutical formulation is delivered to the human by one actuation of the device into one nostril of the human.
100 . A method of treating opioid overdose or a symptom thereof in a human comprising administering a therapeutically effective amount of the pharmaceutical formulation of claim 85 by a pre-primed, bi-dose device adapted for nasal delivery of the pharmaceutical formulation to said human, wherein:
a first volume of the pharmaceutical formulation is present in a first reservoir,
a second volume of the pharmaceutical formulation is present in a second reservoir, and
the therapeutically effective amount of the nalmefene is delivered essentially by a first actuation of the drug delivery device from the first reservoir into a nostril of the human and a second actuation of the drug delivery device from the second reservoir into a nostril of the human.