Intranasal pharmaceutical dosage forms comprising naloxone
The present invention relates to an intranasal pharmaceutical dosage form comprising a dosing unit comprising naloxone or a pharmaceutically acceptable salt thereof in an amount of equivalent to ≥0.5 mg naloxone HC dissolved in an application fluid of a volume of ≤250 μl. Furthermore, the present invention relates to such an intranasal pharmaceutical dosage form for use in the treatment of opioid overdosing and/or at least one symptom thereof.
1. A method of treating opioid overdosing or at least one symptom thereof, the method comprising intranasally administering a patient in need thereof 100 μl of an intranasal pharmaceutical dosage form comprising naloxone or a pharmaceutically acceptable salt thereof dissolved in an aqueous application fluid in a final concentration equivalent to between 18 mg naloxone HCl per ml aqueous application fluid and 50 mg naloxone HCl per ml aqueous application fluid, wherein the dosage form has a pH of ≤5.5 and does not include a permeability enhancer.
2. The method of claim 1 , wherein the final concentration of the naloxone or pharmaceutically acceptable salt thereof is equivalent to between 20 mg naloxone HCl per ml aqueous application fluid and 60 mg naloxone HCl per ml application fluid.
3. The method of claim 1 , wherein the final concentration of the naloxone or pharmaceutically acceptable salt thereof is equivalent to between 30 mg naloxone HCl per ml aqueous application fluid and 50 mg naloxone HCl per ml application fluid.
4. The method of claim 1 , wherein the final concentration of the naloxone or pharmaceutically acceptable salt thereof is equivalent to 40 mg naloxone HCl per ml aqueous application fluid.
5. The method of claim 1 , wherein the aqueous application fluid is water or an aqueous saline solution.
6. The method of claim 1 , wherein the dosage form is provided in a single dosing unit or two dosing units, dependent on whether the dosage form is provided by administration to one nostril or by administration to two nostrils.
7. The method of claim 1 , wherein the dosage form is a nasal spray, a nasal mucoadhesive dosage form, or a mucosal atomizer device.
8. The method of claim 1 , wherein the naloxone or pharmaceutically acceptable salt thereof is the only pharmaceutically active compound in the dosage form.
9. The method of claim 1 , wherein the dosage form is co-administered with an intramuscular and/or intravenous dosage form comprising naloxone or a pharmaceutically acceptable salt thereof.
10. The method of claim 7 , wherein the dosage form is provided in a single dosing unit for administration administered to one nostril.
11. A method of treating opioid overdosing, the method comprising intranasally administering a patient in need thereof 100 μl of an intranasal pharmaceutical dosage form comprising naloxone or a pharmaceutically acceptable salt thereof dissolved in an aqueous fluid in a final concentration equivalent to 20 mg, 30 mg or 40 mg naloxone HCl per ml aqueous fluid and 50 mg naloxone HCl per ml aqueous fluid, wherein the dosage form has a pH of ≤5.5 and does not include a permeability enhancer.
12. A method of treating opioid overdosing, the method comprising (i) intranasally administering to one nostril of a patient in need thereof 100 μl of an intranasal pharmaceutical dosage form comprising naloxone or a pharmaceutically acceptable salt thereof dissolved in an aqueous fluid in a final concentration equivalent to 20 mg, 30 mg or 40 mg naloxone HCl per ml aqueous fluid and 50 mg naloxone HCl per ml aqueous fluid, wherein the dosage form has a pH of ≤5.5 and does not include a permeability enhancer and (ii) optionally repeating administration until an effective amount of naloxone is reached in the systemic circulation of the patient to counter the effect of the opioid.
13. A method of treating opioid overdosing, the method consisting essentially of (i) intranasally administering to one nostril of a patient in need thereof 100 μl of an intranasal pharmaceutical dosage form comprising naloxone or a pharmaceutically acceptable salt thereof dissolved in an aqueous fluid in a final concentration equivalent to 20 mg, 30 mg or 40 mg naloxone HCl per ml aqueous fluid and 50 mg naloxone HCl per ml aqueous fluid, wherein the dosage form has a pH of ≤5.5 and does not include a permeability enhancer and (ii) optionally repeating administration until an effective amount of naloxone is reached in the systemic circulation of the patient to counter the effect of the opioid.