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US4041153A Expired / Lapsed US ⏱️ 0.0 years remaining

Methods and pharmaceutical preparation for the treatment of hypercholesterolaemia

Assignee: Bristol Myers Co
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Filing: 1975-06-02
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Granted: 1977-08-09
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Expires: 1995-06-02
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Abstract

Abstract A composition for treatment of hypercholesterolemia contains clofibrate or a clofibrate derivative, a metal ion contributing compound which forms substantially insoluble metal bile acid salts and, optionally, a basic anion exchange resin. The composition components combine to give synergistic effect.

Inventors

  • 👤 Alan N. Howard

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 13:33
CPC Classifications
A; A61; A61K; A61K9/00; A61K9/14; A61K31/00; A61K31/21; A61K31/215; A61K33/00

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 83 words
A pharmaceutical composition for use in the treatment per os of hypercholesterolemia, which comprises a hypocholesteremic effective amount of (a) a compound selected from p-chlorophenoxyisobutyric acid, the methyl, ethyl, propyl or butyl ester thereof or a sodium, potassium, calcium, magnesium, aluminum, zinc, bismuth or iron salt thereof, and (b) an ingestible non-toxic bismuth salt capable of dissolution in human gastrointestinal juices, the total amount of non-toxic metal being from 3.2 to 90 equivalents per mole of p-chlorophenoxyisobutyric acid or ester or salt thereof.
Claim 2
Dependent Claim 83 words
A pharmaceutical composition for use in the treatment per os of hypercholesterolemia, which comprises a hypocholesteremic effective amount of (a) a compound selected from p-chlorophenoxyisobutyric acid, the methyl, ethyl, propyl or butyl ester thereof or a sodium, potassium, calcium, magnesium, aluminum, zinc, bismuth or iron salt thereof, and (b) an ingestible non-toxic bismuth salt capable of dissolution in human gastrointestinal juices, the total amount of non-toxic metal being from 3.2 to 90 equivalents per mole of p-chlorophenoxyisobutyric acid or ester or salt thereof.
Claim 3
Dependent Claim 29 words
A composition according to claim 1 wherein the total amount of non-toxic metal is from 4 to 15 equivalents per mole of p-chlorophenoxyisobutyric acid or ester or salt thereof.
Claim 4
Dependent Claim 39 words
A composition according to claim 1 wherein there is also present one or more ingestible non-toxic basic anion exchange resins, there being from 50 to 8000 grams of resin per mole of p-chlorophenoxyisobutyric acid or ester or salt thereof.
Claim 5
Dependent Claim 20 words
A composition according to claim 3 wherein the anion exchange resin is selected from cholestyramine, colestipol or poly-[2-(diethylamino)ethyl]-polyglycerylene dextran hydrochloride.
Claim 6
Dependent Claim 12 words
A composition according to claim 1 comprising ethyl p-chlorophenoxyisobutyrate and bismuth hydroxide.
Claim 7
Independent Claim 90 words
A method for the treatment of hypercholesterolemia, in which there is administered to the patient per os a hypocholesteremic effective dose of a pharmaceutical composition comprising (a) a compound selected from p-chlorophenoxyisobutyric acid, the methyl, ethyl, propyl or butyl ester thereof or a sodium, potassium, calcium, magnesium, aluminum, zinc, bismuth or iron salt thereof, and (b) an ingestible non-toxic bismuth salt capable of dissolution in human gastrointestinal juices, the total amount of non-toxic metal being from 3.2 to 90 equivalents per mole of p-chlorophenoxyisobutyric acid or ester or salt thereof.
Claim 8
Independent Claim 90 words
A method for the treatment of hypercholesterolemia, in which there is administered to the patient per os a hypocholesteremic effective dose of a pharmaceutical composition comprising (a) a compound selected from p-chlorophenoxyisobutyric acid, the methyl, ethyl, propyl or butyl ester thereof or a sodium, potassium, calcium, magnesium, aluminum, zinc, bismuth or iron salt thereof, and (b) an ingestible non-toxic bismuth salt capable of dissolution in human gastrointestinal juices, the total amount of non-toxic metal being from 3.2 to 90 equivalents per mole of p-chlorophenoxyisobutyric acid or ester or salt thereof.
Claim 9
Dependent Claim 31 words
A method according to claim 6 wherein the composition contains a total amount of non-toxic metal from 4 to 15 equivalents per mole of p-chlorophenoxyisobutyric acid or ester or salt thereof.
Claim 10
Dependent Claim 39 words
A method according to claim 6 wherein the composition also contains one or more ingestible non-toxic basic anion exchange resins, there being from 50 to 8000 grams of resin per mole of p-chlorophenoxyisobutyric acid or ester or salt thereof.
Claim 11
Dependent Claim 20 words
A method according to claim 8 wherein the anion exchange resin is selected from cholestyramine, colestipol or poly-[2-(diethylamino)ethyl]-polyglycerylene dextran hydrochloride.
Claim 12
Dependent Claim 42 words
A method according to claim 6 wherein the composition comprises ethyl p-chlorophenoxyisobutyrate and bismuth hydroxide, said composition being administered in an amount sufficient to provide a daily dosage of about 1.5 g. of ethyl p-chlorophenoxyisobutyrate and about 2.0 g. of bismuth hydroxide.

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) 1980-08-08 1981-02-07 1981-08-09 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-08-08 1985-02-07 1985-08-09 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-08-08 1989-02-07 1989-08-09 $7700.00 Window Closed / Lapsed

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