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US4973594A Expired / Lapsed US ⏱️ 0.0 years remaining

Medicaments

Assignee: Glaxo Group Ltd
•
Filing: 1987-12-16
•
Granted: 1990-11-27
•
Expires: 2007-12-16
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Abstract

Abstract The invention relates to the use of compounds which act as antagonists of 5-hydroxytryptamine (5-HT) at 5-HT 3 receptors for the treatment of depression.

Inventors

  • 👤 Michael B. Tyers

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 20:26
CPC Classifications
A; A61; A61K; A61K31/00; A61K31/33; A61K31/395; A61K31/435; A61K31/46; A61K31/41; A61K31/415; A61K31/44; A61K31/445; A61K31/495; A61K31/50; A61K31/55; A61P; A61P25/00; A61P25/24; A61P25/26

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 123 words
A method of treatment of depression which comprises administering to a human or animal subject suffering from depression an effective amount for the treatment of depression of a compound of formula (1): ##STR12## wherein R 1 and R 2 independently represent hydrogen, halogen, C 1-4 alkyl, C 1-4 alkoxy, hydroxy, amino, C 1-4 alkylamino, di(C 1-4 )alkylamino, mercapto or C 1-4 alkylthio; R 3 represents hydrogen, C 1-4 alkyl, C 3-5 alkenyl, aryl or aralkyl; R 4 represents hydrogen, C 1-7 alkyl, C 3-5 alkenyl, or aralkyl; n is 2 or 3; the free valence is attached to either fused ring, and the azabicyclic ring is in either the exo or endo configuration; or an acid addition salt or quaternary ammonium salt thereof.
Claim 2
Independent Claim 123 words
A method of treatment of depression which comprises administering to a human or animal subject suffering from depression an effective amount for the treatment of depression of a compound of formula (1): ##STR12## wherein R 1 and R 2 independently represent hydrogen, halogen, C 1-4 alkyl, C 1-4 alkoxy, hydroxy, amino, C 1-4 alkylamino, di(C 1-4 )alkylamino, mercapto or C 1-4 alkylthio; R 3 represents hydrogen, C 1-4 alkyl, C 3-5 alkenyl, aryl or aralkyl; R 4 represents hydrogen, C 1-7 alkyl, C 3-5 alkenyl, or aralkyl; n is 2 or 3; the free valence is attached to either fused ring, and the azabicyclic ring is in either the exo or endo configuration; or an acid addition salt or quaternary ammonium salt thereof.
Claim 3
Dependent Claim 25 words
A method according to claim 1 wherein the compound of formula (i) is (3 α-tropanyl)-1H-indole-3-carboxylic acid ester or a physiologically acceptable salt or solvate thereof.
Claim 4
Dependent Claim 69 words
A method according to claim 1 in which the compound is a compound of formula (i) wherein R 1 and R 2 indpendently represent hydrogen, halogen or C 1-4 alkyl; R 3 represents hydrogen or C C 1-4 alkyl; R 4 represents hydrogen, C 1-7 alkyl or aralkyl; the carbonyl group is attached to the 3-position of the indole ring, and the azabicyclic ring is in the endo configuration.
Claim 5
Dependent Claim 30 words
A method according to claim 1, wherein said compound of formula (i) is administered in a dose of 0.5 μg to 20 mg from 1 to 4 times per day.
Claim 6
Dependent Claim 30 words
A method according to claim 1 wherein said compound of formula (i) is administered in a dose of 0.05 mg to 10 mg from 1 to 4 times per day.

References Cited (Backward Citations)

GB2125398A Cited
US4803199A Cited
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GB2193633A Cited
US4835173A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1993-11-26 1994-05-28 1994-11-27 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1997-11-26 1998-05-28 1998-11-27 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2001-11-26 2002-05-28 2002-11-27 $7700.00 Window Closed / Lapsed

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