Title:  Systemic use of 5-HT3 receptor antagonists against rheumatic inflammatory processes

United States Patent:  6,384,042

Appl. No.:  931679

Foreign Application Priority Data:  Feb 18, 1999[GB] (9903755); Jun 25, 1999[GB]  (9914947)

The present invention relates to a new use for compounds having 5-HT₃ (serotonin M) receptor antagonist activity, especially tropisetron, for the manufacture of a pharmaceutical composition for the systemic treatment of an inflammatory rheumatic or rheumatoid disease other than crystal induced arthritis and other than living pathogen induced inflammatory diseases as long as the living pathogen is still present.

Description of the Invention

The present invention relates to a new use, in particular a new pharmaceutical use for compounds having 5-HT₃ (serotonin M) receptor, in particular specific 5-HT₃ receptor, antagonist activity, especially in the manufacture of a pharmaceutical composition.

The 5-HT₃ -receptor antagonists comprise a defined and recognised class of pharmaceutically active compounds well known in the art and characterised, as their name implies, by their pharmacological activity. Various 5-HT₃ receptor antagonist compounds are commercially available and clinically applied, e.g. in the treatment of emesis.

In accordance with the present invention it has now surprisingly been found that 5-HT₃ receptor antagonists are useful for the systemic treatment of inflammatory rheumatic or rheumatoid diseases other than crystal induced arthritis, especially gout, and from living pathogen induced inflammatory diseases as long as the living pathogen is still present, especially of inflammation, e.g. of inflammatory processes, conditions, events and disease as well as their sequelae or symptoms, associated with rheumatic or rheumatoid diseases.

Hence, the present invention relates to the use of a 5-HT₃ receptor antagonist or of a pharmaceutically acceptable salt of such an antagonist for the manufacture of a pharmaceutical composition for the systemic treatment of an inflammatory rheumatic or rheumatoid disease other than crystal induced arthritis and other than living pathogen induced inflammatory diseases as long as the living pathogen is still present, for example the treatment of any process, condition, event, or disease as hereinafter described. In particular, the present invention provides the use as mentioned before where, in addition to pain, at least one further sequela or symptom in addition to pain that is associated with the inflammatory rheumatoid or rheumatic disease is alleviated, ameliorated or controlled.

Any 5-HT₃ receptor antagonist can be used in accordance with the invention. Preferred 5-HT₃ receptor antagonists which may be employed in accordance with the present invention are:

A) Ondansetron [1,2,3,9-tetrahydro-9-methyl-3-[(2-methyl-IH-imidazol-1-yl]methyl]-4H-carb azol-4-one (cf. Merck Index, twelfth edition, item 6979);

B) Granisetron [endo-1-methyl-N-(9-methyl-9-aza-bicyclo[3.3. 1]non-3-yl)-IH-imidazole-3-carboxamide: (cf. loc. cit., item 4557); and

C) Dolasetron [IH-indole-3-carboxylic acid (2.alpha., 6.alpha., 8.alpha., 9.alpha..beta.)-octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester] (cf. loc. cit., item 3471).

Particular 5-HT₃ receptor antagonists which may be employed in accordance with the present invention are those of the formula 1 as defined in European Patent Publication 189002 B1, the contents of which are incorporated herein by reference, in particular the compound:

D) Indol-3-yl-carboxylic acid-endo-8-methyl-8-aza-bicyclo[3,2,1]-oct-3-yl-ester, also known as tropisetron. (cf. loc.cit., item 9914).

Further 5-HT₃ receptor antagonists which may be used preferably in accordance with the present invention are:

E) 4,5,6,7-tetrahydro-5-[(1-methyl-indol-3-yl)carbonyl]benzimidazole (see also ramosetron, see U.S. Pat. No. 5,344,927);

F) (+)-10-methyl-7-(5-methyl-1H-imidazol-4-ylmethyl)-6,7,8,9-tetrahydropyrido [1,2-a]indol-6-one (see also fabesetron, EP 0 361 317); and

G) [N-(1-ethyl-2-imidazolin-2-yl-methyl)-2-methoxy-4-amino-5-chlorobenzamide (see also lintopride-Chem.- Abstr.-No. 107429-63-0).

A further 5-HT₃ receptor antagonists which may be used preferably in accordance with the present invention is

H) 2,3,4,5-tetrahydro-5-methyl-2-[(5-methyl-1H-imidazol-4-yl)methyl]-1H-pyrid o[4,3-b]indol-1-one (see also alosetron, EP 0 306 323).

Each of these compounds, alone or in combination with one or more other 5-HT₃ inhibitor, may be used for the treatment according to the invention.

For use in accordance with the present invention tropisteron (especially in the formulation called NAVOBAN.RTM.) is most preferred.

5-HT₃ -receptor antagonists may be employed in accordance with the invention in free or in pharmaceutically acceptable salt form, e.g. as known in the art, for example, in the case of compounds A) to D) above in pharmaceutically acceptable acid addition salt form, for example, in the case of: compound A) the hydrochloride dihydrate; compound B) the hydrochloride; compound C) the mesylate; and compound D) the monohydrochloride. References to 5-HT₃ receptor antagonists collectively or individually throughout the present specification and claims are accordingly to be understood as embracing both free compounds and such pharmaceutically acceptable salt forms, e.g. as clinically employed, and further also solvates, e.g. hydrates, or specific crystal forms of any of these compounds or salts.

Thus, the invention relates to the use of a 5-HT₃ receptor antagonist or of a pharmaceutically acceptable salt of such an antagonist for the manufacture of a pharmaceutical composition for the systemic treatment of an inflammatory rheumatic or rheumatoid disease other than crystal induced arthritis and other than living pathogen induced inflammatory diseases as long as the living pathogen is still present, where the 5-HT₃ receptor antagonist is selected from the group consisting of ondansetron, granisetron, dolasetron, tropisetron, ramosetron, fabesetron, lintopride and alosetron, which may be used in free form, that is, not as a salt, or as a pharmaceutically acceptable salt.

In accordance with the present invention it has now surprisingly been found that 5-HT₃ receptor antagonists are useful for the treatment of inflammation. They are useful for the treatment of inflammatory rheumatic or rheumatoid processes, conditions or events, for example, consequential to disease (including infection, for example viral infection, with the proviso that in case of an acute infection or parasite infestation, e.g. bacterial, fungal or, in a broader sense, viral or protozoal infection, or infestation by a parasite, first treatment of the infection or infestation itself, e.g. with antibiotics or other treatment, is indicated to remove the living pathogen before the 5-HT₃ antagonist is used), as well for the treatment of inflammatory disease as such.

"Treatment" as used herein includes systemic use for the alleviation, amelioration or control of inflammation, e.g. of inflammatory rheumatic or rheumatoid disease, process, condition or event. It also includes intervention for the alleviation, amelioration or control of the sequelae or symptoms of inflammation, for example degeneration (e.g. of cells, epithelia or tissues), or especially swelling, exudation or effusion, or pain. In this context the term "treatment" is further to be understood as embracing use to reverse, restrict or control progression of any specified disease, process, condition, event or the like, including use for disease modifying effect. If any of the mentioned diseases, processes, conditions or events is associated with pain, the term "treatment" preferably encompasses the alleviation, amelioration or control (including temporal or permanent removal) of at least one further sequela or symptom in addition to pain, such as swelling, effusion, exsudation, stiffness, lack of flexibility of joints, or degeneration, more preferably of all symptoms and most preferably of the total clinical picture of the respective disease, irritation or manifestation.

The present invention is in particular applicable to the systemic treatment of an inflammatory disease other than crystal induced arthritis (gout) or preferably other than living pathogen induced inflammation as long as the living pathogen is still present, especially of manifestations at the locomotor apparatus, such as various inflammatory rheumatoid diseases (except for crystal induced arthritis (e.g. gout) and living pathogen induced diseases as long as the pathogen (e.g. a virus, bacterium, fungus, protozoon or parasite) is still present, so that causal treatment against the pathogen is indicated first, such as

(1) chronic polyarthritis (=rheumatoid arthritis), including juvenile arthritis or psoriasis arthropathy;

(2) paraneoplastic syndrome or tumor-induced inflammatory diseases,

(3) turbid effusions,

(4) collagenosis, such as systemic Lupus erythematosus, poly-myositis, dermato-myositis, systemic sclerodermia or mixed collagenosis;

(5) postinfectious arthritis (where no living pathogenic organism can be found at or in the affected part of the body), or

(6) seronegative spondylarthritis, such as spondylitis ankylosans;

or further

(7) vasculitis,

(8) sarcoidosis, or

(9) arthrosis;

or further any combinations thereof.

An example of a preferred inflammation to be treated systemically is

a) synovial inflammation, for example, synovitis, including any of the particular forms of synovitis recited in Dorland's Illustrated Medical Dictionary, 26th edition, pub. W. B. Saunders and Co. at page 1301, in particular bursal synovitis and purulent synovitis, as far as it is not crystal-induced. Such synovial inflammation may for example, be consequential to or associated with disease, e.g. arthrosis, including arthritis, e.g. osteoarthritis, rheumatoid arthritis or arthritis deformans.

The present invention is further applicable to the systemic treatment of:

b) Inflammation, e.g. inflammatory diseases or conditions, of the joints or locomotor apparatus in the region of the tendon insertions and tendon sheaths.

Such inflammation may, for example, be consequential to or associated with disease or further (in a broader sense of the invention) with surgical intervention, e.g. as recited under a) above, including, in particular conditions such as insertion endopathy, myofasciale syndrome and tendomyosis.

The present invention is especially applicable to the treatment of:

c) Inflammation, e.g. inflammatory disease or condition, of connective tissues.

Such diseases or conditions include in particular dermatomyositis and myositis.

From the foregoing it will be understood that the present invention is to be further understood as embracing the systemic treatment, e.g. therapy, of any disease or condition as set forth above, for example arthrosis, dermatomyositis etc., for example, for the alleviation or control of inflammatory processes or events and their sequelae associated therewith or consequential thereto, e.g. for the treatment of rheumatoid arthritis, e.g. to alleviate or control joint inflammation or effusion.

In the case of the inflammatory diseases, diseases where a living pathogen, e.g. a virus, a bacterium, a fungus, a protozoon or a parasite or the like, is still present, the treatment of must first aim at removal of the pathogen causative for the disease, before treatment with a 5-HT₃ antagonist is used, as otherwise there is the danger that the causative pathogen remains intact. Then the mere symptomatic treatment with a 5-HT₃ antagonist is contraindicated in order to avoid survival or even further spread of the causative infection. This is also valid in the case of combination with an anti-inflammatory glucocorticosteroid as described in the following, as is the proviso that treatment of crystal-induced inflammation is excluded.

In a further aspect it has been found in accordance with the present invention that systemic administration of 5-HT₃ receptor antagonists is useful as replacement therapy for anti-inflammatory glucocorticosteroid, e.g. cortisone or the like, therapy. For example for use in any means of treatment as hereinbefore set forth.

The term "replacement therapy" as used herein is to be understood as embracing both use "as full replacement", i.e. use instead of anti-inflammatory glucocorticosteroid therapy, as well as use "as partial replacement" for anti-inflammatory glucocorticosteroid therapy, i.e. for administration together with anti-inflammatory glucocorticosteroid therapy or as a means of reducing glucocorticosteroid dosage or to achieve a glucocorticosteroid sparing effect.

The present invention accordingly provides:

I. A method of treating inflammation, for example treating any process, condition, event, or disease as hereinbefore set forth, in a subject in need thereof, which method comprises administering systemically an effective amount of a 5-HT₃ receptor antagonist;

II. A method of providing replacement therapy for anti-inflammatory glucocorticosteroid therapy in a subject receiving such glucocorticosteroid therapy, for example for or in the treatment of any process, condition, event or disease as hereinbefore set forth, which process comprises systemicalls administering to said subject an effective amount, e.g. an anti-inflammatory glucocorticosteroid sparing amount, of a 5-HT₃ -receptor antagonist; as well as

III. A method of treating inflammation, for example treating any process, condition, event or disease as hereinbefore set forth, in a subject in need thereof, which method comprises systemically administering an effective amount of a 5-HT₃ receptor antagonist together with an anti-inflammatory glucocorticosteroid.

Where co-administration is practiced as under III above the drug substances, i.e. 5-HT₃ receptor antagonist and anti-inflammatory glucocorticosteroid may be administered sequentially or simultaneously or substantially simultaneously, e.g. employing a fixed combination dosage form.

In further aspects the present invention also provides:

IV. A 5-HT₃ receptor antagonist for use in, or for use in the manufacture of a pharmaceutical composition for use in; or the use of a pharmaceutical composition comprising a 5-HT₃ receptor antagonist for systemic use:

a) in the treatment of inflammation, for example any inflammatory process, condition, event or disease as hereinbefore set forth;

b) as replacement therapy for anti-inflammatory glucocorticosteroid therapy, for example in the treatment of any inflammatory process, condition, event or disease as hereinbefore set forth; or

c) for co-administration together with an anti-inflammatory glucocorticosteroid in the treatment of inflammation, for example in the treatment of any inflammatory process, condition, event or disease as hereinbefore set forth; as well as

V. A pharmaceutical dosage form for systemic administration comprising a 5-HT₃ receptor antagonist together with an anti-inflammatory glucocorticosteroid.

The terms "systemically administering" or "systemic use" refer to a way of administration that is not local (=at or near the site of a disease manifestation), but that leads to exposure of most or all of the parts of the body to the 5-HT₃ -antagonist.

Dosage forms in accordance with V above are to be understood as including both fixed-unit-dosage forms, e.g. tablets, capsules, liquid formulations and the like comprising both active ingredients together with appropriate pharmaceutically acceptable diluents or carriers, as well as twin delivery systems, packages or the like comprising both active ingredients separately or in separate dosage form, for concommitant or sequential administration.

Claim 1 of 10 Claims

What is claimed is:

1. A method for systemic treatment of an inflammatory rheumatic or rheumatoid disease or condition, other than crystal induced arthritis and other than living pathogen induced inflammatory diseases, as long as the living pathogen is still present comprising administering a therapeutically effective amount of a 5-HT₃ receptor antagonist or a pharmaceutically acceptable salt thereof to a subject in need thereof, wherein the disease to be treated is selected from the group consisting of:

(1) chronic polyarthritis,

(2) paraneoplastic syndrome or tumor-induced inflammatory diseases,

(3) turbid effusions,

(4) collagenosis,

(5) postinfectious arthritis,

(6) seronegative spondylarthritis,

(7) vasculitis,

(8) sarcoidosis, and

(9) arthrosis.

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