TOPICAL TRANSDERMAL DEXMEDETOMIDINE COMPOSITIONS AND METHODS OF USE THEREOF
Analgesic topical formulations of dexmedetomidine and methods of use thereof in the treatment and management of pain and other conditions.
1 . A method of treating or preventing pain comprising
applying to the skin of the mammal a composition comprising a dosage of dexmedetomidine or a pharmaceutically acceptable salt or pro-drug thereof in a pharmaceutically acceptable vehicle,
wherein the dexmedetomidine or pharmaceutically acceptable salt or pro-drug thereof is absorbed through the skin and produces analgesia without sedation.
2 . The method according to claim 1 , wherein said dosage of dexmedetomidine or pharmaceutically acceptable salt thereof is between about 0.05 μg/kg and about 15 mcg/kg, and wherein said mammal is a human.
3 . The method according to claim 2 , wherein said mammal is a human, and said transdermal dosage of dexmedetomidine or pharmaceutically acceptable salt thereof is between about 100 μg and about 1500 μg.
4 . The method according to claim 3 , wherein the plasma c max of dexmedetomidine upon absorption from transdermal application and into the systemic circulatory system of said human is less than about 0.30 ng/mL.
5 . The method according to claim 2 , wherein said applying step comprises topically applying said pharmaceutical composition to the skin of at least one of the legs, arms, abdomen, chest, groin, neck, back, and shoulders.
6 . The method according to claim 5 , wherein said applying step comprises applying a cream, lotion, or gel of the pharmaceutical composition to said skin of said mammal.
7 . The method according to claim 6 , wherein said applying step does not require covering of the skin with a dressing after administration of said pharmaceutical composition onto the skin of said mammal.
8 . The method according to claim 2 , wherein, during at least the 6 hours immediately after applying said pharmaceutical composition, the resting mean arterial blood pressure of the human varies by no more than about 20 mmHg.
9 . The method according to claim 2 , wherein, during the at least the 6 hours immediately after applying said pharmaceutical composition, said human is able to remain awake and to respond to commands, and said human is alert and oriented.
10 . The method according to claim 1 , wherein said dexmedetomidine or pharmaceutically acceptable salt thereof is co-administered with one or more other analgesics.
11 . The method according to claim 10 , wherein said pharmaceutical composition is administered intermittently to treat breakthrough pain that is inadequately controlled by said one or more other analgesics.
12 . The method according to claim 2 , wherein said pain is idiopathic pain.
13 . The method according to claim 12 , wherein said idiopathic pain is selected from the group consisting of neuralgia, myalgia, hyperalgia, hyperpathia, neuritis, and neuropathy.
14 . The method according to claim 2 , wherein said pain is associated with or caused by cancer, viral infection, physical trauma, arthritis, headache, or lower back pain.
15 . The method according to claim 14 , wherein said physical trauma is associated with or caused by surgery, a burn, or blunt force trauma.
16 . A method of treating or preventing pain comprising
applying to a skin membrane of a mammal a pharmaceutical composition comprising dexmedetomidine, or a pharmaceutically acceptable salt or pro-drug thereof, in a pharmaceutically acceptable vehicle,
wherein said dexmedetomidine, or said pharmaceutically acceptable salt or pro-drug thereof, is absorbed through said skin and produces analgesia without sedation.
17 . A method of treating or preventing pain comprising
administering to the skin of a mammal a systemically absorbed pharmaceutical composition comprising dexmedetomidine, or a pharmaceutically acceptable salt or pro-drug thereof, in an amount effective to treat or to prevent pain in said mammal upon administration,
wherein said pharmaceutical composition provides a physiologically active amount of dexmedetomidine into the systemic circulatory system of said mammal at a rate that produces an analgesic effect without sedation within at least 6 hours of administration.
18 . An analgesic pharmaceutical composition comprising dexmedetomidine, or a pharmaceutically acceptable salt or pro-drug thereof, in a pharmaceutically acceptable vehicle, said pharmaceutical composition being configured and adapted for topical administration to a mammal by applying said analgesic pharmaceutical composition to the skin of said mammal.
19 . The analgesic pharmaceutical composition according to claim 18 , wherein said analgesic pharmaceutical composition is configured and adapted for topical administration by applying said composition to the skin more that once daily.
20 . The analgesic pharmaceutical composition according to claim 18 , wherein said analgesic pharmaceutical composition is configured and adapted for topical administration by applying said composition to the skin of at least one of the legs, arms, abdomen, chest, groin, neck, back, and shoulders of said mammal.
21 . The analgesic pharmaceutical composition according to claim 18 , wherein said pharmaceutically acceptable salt of dexmedetomidine is dexmedetomidine hydrochloride, and wherein said vehicle is selected from at least one of creams, gels, and suspensions.
22 . The analgesic pharmaceutical composition according to claim 21 , wherein the composition does not require an occlusion or covering after administration onto the skin of a mammal.
23 . The analgesic pharmaceutical composition according to claim 18 , wherein said analgesic pharmaceutical composition is packaged in a dispensing device.
24 . An apparatus for treating or preventing pain, said apparatus comprising
an analgesic pharmaceutical composition comprising dexmedetomidine, or a pharmaceutically acceptable salt or pro-drug thereof, in a pharmaceutically acceptable vehicle, and
a dispensing device that contains and dispenses said analgesic pharmaceutical composition.
25 . The apparatus of claim 24 , wherein the apparatus includes an applicator configured and arranged for conveying the composition from the apparatus to the skin of a mammal.