US2005164997A1PendingUtilityA1
Pharmaceutical formulation for administration by inhalation comprising an androstane derivative and a beta-2-adrenoreceptor for the treatment of inflammatory and allergic conditions
Priority: Aug 5, 2000Filed: Feb 4, 2003Published: Jul 28, 2005
Est. expiryAug 5, 2020(expired)· nominal 20-yr term from priority
Inventors:Keith Biggadike
A61P 37/08A61P 29/00A61P 11/06A61K 9/008A61P 11/00A61K 31/58A61K 45/06A61K 31/00A61K 31/137A61K 9/0075
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Claims
Abstract
A pharmaceutical formulation for administration by inhalation comprising a compound of formula (I), or a solvate thereof, together with a long-acting β 2 -adrenoreceptor agonist which formulation has a therapeutically useful effect in the treatment of inflammatory disorders of the respiratory tract over a period of 24 hours or more.
Claims
exact text as granted — not AI-modified1 . A pharmaceutical formulation for administration by inhalation comprising a compound of formula (I),
or a solvate thereof, together with a long-acting β 2 -adrenoreceptor agonist, wherein the β 2 -adrenoreceptor agonist is a compound of the formula (M):
or a salt or solvate thereof, wherein:
m is an integer of from 2 to 8.
n is an integer of from 3 to 11.
with the proviso that m+n is 5 to 19,
R 11 is —XSO 2 NR 16 R 17 wherein X is —(CH 2 ) p - or C 2-6 alkenylene;
R 16 and R 17 are independently selected from hydrogen, C 1-6 alkyl, C 3-7 cycloalkyl, C(O)NR 18 R 19 , phenyl, and phenyl (C 1-4 alkyl)-,
or R 16 and R 17 , together with the nitrogen to which they are bonded, form a 5-, 6-, or 7-membered nitrogen containing ring, and R 16 and R 17 are each optionally substituted by one or two groups selected from halo, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, hydroxy-substituted C 1-6 alkoxy, —CO 2 R 18 , —SO 2 NR 18 R 19 , —CONR 18 R 19 , —NR 18 C(O)R 19 , or a 5-, 6- or 7-membered heterocylic ring,
R 18 and R 19 are independently selected from hydrogen, C 1-6 alkyl,
C 3-6 cycloalkyl, phenyl, and phenyl (C 1-4 alkyl)-; and
p is an integer of from 0 to 6, preferably from 0 to 4;
R 12 and R 13 are independently selected from hydrogen, C 1-6 alkyl, C 1-6 alkoxy, halo, phenyl, and C 1-6 -haloalkyl; and
R 14 and R 15 are independently selected from hydrogen and C 1-4 alkyl with the proviso that the total number of carbon atoms in R 14 and R 15 is not more than 4,
which formulation has a therapeutically useful effect in the treatment of inflammatory disorders of the respiratory tract over a period of 24 hours or more.
2 . A pharmaceutical formulation according to claim 1 wherein the compound of formula (I) or a solvate thereof and the long-acting β 2 -adrenoreceptor agonist are both present in particulate form.
3 . A pharmaceutical formulation according to claim 2 further comprising a particulate carrier.
4 . A pharmaceutical formulation according to claim 3 wherein the carrier is lactose.
5 . A pharmaceutical formulation according to claim 1 further comprising a liquified propellant gas.
6 . A pharmaceutical formulation according to claim 1 wherein the inflammatory disorder of the respiratory tract is asthma.
7 . (canceled)
8 . A method of treatment of an inflammatory disorder of the respiratory tract once-per-day which comprises administration of a pharmaceutical formulation according to claim 1 .
9 . A method of treatment according to claim 8 wherein the inflammatory disorder of the respiratory tract is asthma.
10 . An inhaler containing a plurality of doses of a pharmaceutical formulation comprising a compound of formula (I)
or a solvate thereof, together with a long-acting β 2 -adrenoreceptor agonist, wherein the β 2 -adrenoreceptor agonist is a compound of the formula (M):
or a salt or solvate thereof, wherein:
m is an integer of from 2 to 8.
n is an integer of from 3 to 11,
with the proviso that m+n is 5 to 19,
R 11 is —XSO 2 NR 16 R 17 wherein X is —(CH 2 ) p - or C 2-6 alkenylene;
R 16 and R 17 are independently selected from hydrogen, C 1-6 alkyl, C 3-7 cycloalkyl, C(O)NR 18 R 19 , phenyl, and phenyl (C 1-4 alkyl)-,
or R 16 and R 17 , together with the nitrogen to which they are bonded, form a 5-, 6-, or 7-membered nitrogen containing ring, and R 16 and R 17 are each optionally substituted by one or two groups selected from halo, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, hydroxy-substituted C 1-6 alkoxy, —CO 2 R 18 —SO 2 NR 18 R 19 , —CONR 18 R 19 , —NR 18 C(O)R 19 , or a 5-, 6- or 7-membered heterocylic ring,
R 18 and R 19 are independently selected from hydrogen, C 1-6 alkyl, C 3-6 cycloalkyl, phenyl, and phenyl (C 1-4 alkyl)-; and
p is an integer of from 0 to 6, preferably from 0 to 4;
R 12 and R 13 are independently selected from hydrogen, C 1-6 alkyl, C 1-6 alkoxy, halo, phenyl, and C 1-6 haloalkyl; and
R 14 and R 15 are independently selected from hydrogen and C 1-6 alkyl with the proviso that the total number of carbon atoms in R 14 and R 15 is not more than 4,
which formulation has a therapeutically useful effect in the treatment of inflammatory disorders of the respiratory tract over a period of 24 hours or more, and which doses are suitable for once-per-day administration of the formulation by inhalation.
11 . An inhaler according to claim 10 wherein the compound of formula (I) or a solvate thereof and the long-acting β 2 -adrenoreceptor agonist are both present in particulate form.
12 . An inhaler according to claim 10 wherein the formulation further comprises a particulate carrier.
13 . An inhaler according to claim 12 wherein the carrier is lactose.
14 . An inhaler according to claim 10 wherein the formulation further comprises a liquefied propellant gas.
15 . (canceled)
16 . An inhaler according to claim 10 wherein the inflammatory disorder of the respiratory tract is asthma.
17 - 19 . (canceled)
20 . A method for the treatment of a human or animal subject with an anti-inflammatory and/or allergic condition, which method comprises administering to said human or animal subject an effective amount of a formulation as claimed in claim 1.Join the waitlist — get patent alerts
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