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US5627206A Expired / Lapsed US ⏱️ 0.0 years remaining

Tricyclic inhibitor of matrix metalloproteinases

Assignee: Warner Lambert Co LLC
•
Filing: 1995-06-02
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Granted: 1997-05-06
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Expires: 2015-06-02
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Abstract

Abstract A tricyclic compound is described as well as pharmaceutical compositions of same, which is useful as an inhibitor of matrix metalloproteinases, particularly gelatinase A (72 kD gelatinase) for the treatment of multiple sclerosis or other autoimmune or inflammatory disorders dependent upon tissue invasion by leukocytes.

Inventors

  • 👤 Donald Hupe
  • 👤 Linda Lea Johnson
  • 👤 Qi-Zhuang Ye

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-08 17:40
CPC Classifications
C; C07; C07D; C07D307/00; C07D307/77; C07D307/91

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 38 words
A method of treating multiple sclerosis comprising administering to a host suffering therefrom a therapeutically effective amount of the compound of Formula I ##STR2## or corresponding isomers thereof; or a pharmaceutically acceptable salt thereof in unit dosage form.
Claim 2
Independent Claim 38 words
A method of treating multiple sclerosis comprising administering to a host suffering therefrom a therapeutically effective amount of the compound of Formula I ##STR2## or corresponding isomers thereof; or a pharmaceutically acceptable salt thereof in unit dosage form.
Claim 3
Independent Claim 46 words
A method of treating autoimmune or inflammatory disorders dependent upon tissue invasion by leukocytes comprising administering to a host suffering therefrom a therapeutically effective amount of the compound of Formula I ##STR3## or corresponding isomers thereof; or a pharmaceutically acceptable salt thereof in unit dosage form.
Claim 4
Independent Claim 46 words
A method of treating autoimmune or inflammatory disorders dependent upon tissue invasion by leukocytes comprising administering to a host suffering therefrom a therapeutically effective amount of the compound of Formula I ##STR3## or corresponding isomers thereof; or a pharmaceutically acceptable salt thereof in unit dosage form.
Claim 5
Dependent Claim 20 words
A pharmaceutical composition comprising the compound of Formula I: ##STR4## in admixture with a pharmaceutically acceptable excipient, diluent, or carrier.
Claim 6
Dependent Claim 20 words
A pharmaceutical composition comprising the compound of Formula I: ##STR4## in admixture with a pharmaceutically acceptable excipient, diluent, or carrier.
Claim 7
Dependent Claim 41 words
A pharmaceutical composition adapted for administration as an agent for treating inflammatory diseases dependent upon tissue invasion by leukocytes comprising a therapeutically effective amount of the compound according to claim 3 in admixture with a pharmaceutically acceptable excipient, diluent, or carrier.
Claim 8
Dependent Claim 35 words
A pharmaceutical composition adapted for administration as an agent for treating multiple sclerosis comprising a therapeutically effective amount of the compound according to claim 3 in admixture with a pharmaceutically acceptable excipient, diluent, or carrier.

References Cited (Backward Citations)

No citation records indexed.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 2000-05-05 2000-11-04 2001-05-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2004-05-05 2004-11-04 2005-05-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2008-05-05 2008-11-04 2009-05-06 $7700.00 Window Closed / Lapsed

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