Deuterated derivatives of ruxolitinib
US-9249149-B2 · Feb 2, 2016 · US
US2020222408A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2020222408-A1 |
| Application number | US-201916704402-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 5, 2019 |
| Priority date | May 4, 2016 |
| Publication date | Jul 16, 2020 |
| Grant date | — |
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or a pharmaceutically acceptable salt thereof. This invention also provides compositions comprising Compound (I) and the use of such compositions in the described methods.
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1 - 31 . (canceled) 32 . A method of treating a hair loss disorder in a human subject, the method comprising administering to the human subject 16 mg/day of a compound represented by the following structural formula: or a pharmaceutically acceptable salt thereof, wherein each position in Compound (I) designated specifically as deuterium has at least 95% incorporation of deuterium. 33 . The method of claim 32 , wherein the hair loss disorder is alopecia areata. 34 . The method of claim 32 , wherein the compound is administered orally. 35 . The method of claim 32 , wherein the compound is administered in a pharmaceutical formulation which is a tablet. 36 . The method of claim 32 , wherein the compound is administered once a day. 37 . The method of claim 32 , wherein the compound is administered twice a day. 38 . The method of claim 37 , wherein the step of administering comprises administering to the subject 8 mg twice per day. 39 . The method of claim 32 , wherein in Compound (I), any atom not designated as deuterium is present at its natural isotopic abundance. 40 . The method of claim 32 , wherein each position in Compound (I) designated specifically as deuterium has at least 97% incorporation of deuterium. 41 . A method of treating a hair loss disorder in a human subject, the method comprising administering to the human subject 24 mg/day of a compound represented by the following structural formula: or a pharmaceutically acceptable salt thereof, wherein each position in Compound (I) designated specifically as deuterium has at least 95% incorporation of deuterium. 42 . The method of claim 41 , wherein the hair loss disorder is alopecia areata. 43 . The method of claim 41 , wherein the compound is administered orally. 44 . The method of claim 41 , wherein the compound is administered in a pharmaceutical formulation which is a tablet. 45 . The method of claim 41 , wherein the compound is administered once a day. 46 . The method of claim 41 , wherein the compound is administered twice a day. 47 . The method of claim 46 , wherein the step of administering comprises administering to the subject 12 mg twice per day. 48 . The method of claim 41 , wherein in Compound (I), any atom not designated as deuterium is present at its natural isotopic abundance. 49 . The method of claim 41 , wherein each position in Compound (I) designated specifically as deuterium has at least 97% incorporation of deuterium. 50 . A pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and 8 mg of a compound represented by the following structural formula: or a pharmaceutically acceptable salt thereof, wherein each position in Compound (I) designated specifically as deuterium has at least 95% incorporation of deuterium. 51 . A pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and 12 mg of a compound represented by the following structural formula: or a pharmaceutically acceptable salt thereof, wherein each position in Compound (I) designated specifically as deuterium has at least 95% incorporation of deuterium.
Pills, tablets, {discs, rods (A61K9/0004, A61K9/0007, A61K9/0056, A61K9/0065 take precedence; for reconstitution of a drink A61K9/0095)} · CPC title
Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose · CPC title
Mouth and digestive tract, i.e. intraoral and peroral administration · CPC title
ortho- or peri-condensed with heterocyclic rings · CPC title
for baldness or alopecia · CPC title
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