US2021032250A1PendingUtilityA1
Glucuronide prodrugs of janus kinase inhibitors
Assignee: THERAVANCE BIOPHARMA R&D IP LLCPriority: May 23, 2017Filed: Jul 13, 2020Published: Feb 4, 2021
Est. expiryMay 23, 2037(~10.8 yrs left)· nominal 20-yr term from priority
C07H 17/02A61P 1/00C07H 15/26C07H 1/00A61P 29/00C07D 487/04A61K 31/7064C07H 13/12
61
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Claims
Abstract
where W1, R1 and A1 are as defined. The invention also relates to pharmaceutical compositions comprising such compounds; methods of using such compounds to treat gastrointestinal inflammatory diseases; and processes and intermediates for preparing such compounds.
Claims
exact text as granted — not AI-modified1 - 72 . (canceled)
73 . A pharmaceutical composition comprising a pharmaceutically acceptable-carrier and a compound of formula VII-1:
or a pharmaceutically acceptable salt thereof.
74 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition is suitable for oral administration.
75 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition is in the form of a capsule.
76 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition is in the form of a tablet.
77 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition is in the form of a pill.
78 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition is in the form of a lozenge, cachet, dragee, granules, emulsion, elixir, or syrup.
79 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition is in the form of a suspension.
80 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition is in the form of a solution.
81 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition is in the form of a powder.
82 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition comprises from about 0.01 to about 95% by weight of the compound of formula VII-1, or a pharmaceutically acceptable salt thereof.
83 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition comprises from about 0.01 to about 30% by weight of the compound of formula VII-1, or a pharmaceutically acceptable salt thereof.
84 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition comprises from about 0.01 to about 10% by weight of the compound of formula VII-1, or a pharmaceutically acceptable salt thereof.
85 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition comprises from about 0.1 to about 10% by weight of the compound of formula VII-1, or a pharmaceutically acceptable salt thereof.
86 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition comprises from about 0.5 to about 5% by weight of the compound of formula VII-1, or a pharmaceutically acceptable salt thereof.
87 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition comprises from about 0.5 to about 50 mg of the compound of formula VII-1, or a pharmaceutically acceptable salt thereof.
88 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition comprises from about 1 to about 40 mg of the compound of formula VII-1, or a pharmaceutically acceptable salt thereof.
89 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition comprises from about 1 to about 20 mg of the compound of formula VII-1, or a pharmaceutically acceptable salt thereof.
90 . The pharmaceutical composition of claim 73 , wherein the pharmaceutical composition comprises one or more additional therapeutic agents.Join the waitlist — get patent alerts
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