GB2200046A - Pharmaceutical compositions for gastric disorders - Google Patents
Pharmaceutical compositions for gastric disorders Download PDFInfo
- Publication number
- GB2200046A GB2200046A GB08727836A GB8727836A GB2200046A GB 2200046 A GB2200046 A GB 2200046A GB 08727836 A GB08727836 A GB 08727836A GB 8727836 A GB8727836 A GB 8727836A GB 2200046 A GB2200046 A GB 2200046A
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- United Kingdom
- Prior art keywords
- sub
- methyl
- pharmaceutical composition
- physiologically acceptable
- tetrahydro
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
Abstract
The invention relates to the use of compounds of the general formula (I)whereinR' represents a hydrogen atom or a C<sub>1-10</sub> alkyl, C<sub>3-7</sub> cycloalkyl, C<sub>3-7</sub> cycloalkyl-(C<sub>1-4</sub>) alkyl, C<sub>3</sub>-<sub>6</sub> alkenyl, C<sub>3-10</sub> alkynyl, phenyl or phenyl-C<sub>1-3</sub> alkyl group; and one of the groups represented byR<sup>2</sup>, R<sup>3</sup> and R<sup>4</sup> is a hydrogen atom or a C<sub>1-3</sub> alkyl, C<sub>3-7</sub>cycloalkyl, C<sub>2-6</sub> alkenyl or phenyl - C<sub>1-3</sub> alkyl group and each of the other two groups, which may be the same or different, represents a hydrogen atom or a C<sub>1-6</sub> alkyl group; and physiologically acceptable salts and solvates thereof, for the relief of nausea and vomiting and/or the promotion of gastric emptying and for the manufacture of a medicament for this purpose. Promotion of gastric emptying may be for the relief of gastro-intestinal disorders associated with gastric stasis or may be of advantage in radiological examination procedures.The invention also relates to a product containing a therapeutic agent liable to induce nausea and vomiting, e.g. a cytostatic agent such as a cyclophosphamide, an alkylating agent or a platinum complex, and a compound of the general formula (1) as a combined preparation for simultaneous separate or sequential use in therapy.
Description
1 v - 1 PHARMACEUTICAL COMPOSITIONS 2'.e"'-00046 This invention relates to
improvements in the formulation of drugs for the treatment of g.astrointestinal disorders. More particularly it relates to pharmaceutical compositions comprising a
compound having antagonist activity at 5HT3 receptors and ranitidine. In our UK Patent Specification No. 2153821A we disclose _inter alia 1,2,3,9tetrahydro-9-methyl-3-[(2-methyl-lH- - imidazol-1-yl) methyl]-4H-carbazol4-one which may be represented by the formula (I)
0 N # Me Me (I) and physiologically acceptable saltsy solvates and physiologically acceptable equivalents thereof.
In the aforementioned specification the compounds are described as potent and selective antagonists of 5-hydroxytryptamine (5HT) at 'neurdnal' 5HT receptors of the type located on terminals of primary afferent nerves, and which are also present in the central nervous system. Receptors of this type are now designated 5HT3 receptors. The compounds are described as being of u. se in the treatment of a human or animal subject suffering from'a condition caused by a disturbance of neuronal 5HT function, for example in the treatment of miqraine pain or a psychotic disorder such as schizoohrenia. The compou I nds may also be useful in the treatment of conditions such as anxiety, obesity and mania.
We have found that the compound of formula (1) additionally promotes gastric emptying and is thus useful in the treatment of conditions which may be relieved by the promotion of gastric emotyina. Such conditions include gastric stasis and symptoms of oastrointestinal dysfunction such as dyspepsia, reflux oesophaqitis, peptic ulcer and flatulence.
- 2 is The compound of formula (I) has also been found to be an anti-emetic, and may be used in the treatment and prevention of nausea and vomiting. The use of the compound of formula (I) for the treatment of emesis is described in published European Patent Specification No. 201165, which specification also refers to the use of the compound of formula (I) for the treatment of irritable bowel syndrome.
Ranitidine is the approved name for N-[2-[[[5-(dimethylamino)methyl]-2furanyllmethyllthio]ethyl-NI-methyl-2-nit ro-1,1ethenediamine which is described and claimed in British Patent Specification No. 1565966. It is a potent histamine H27antaqonist which, in the form of its hydrochloride, is widely used in the treatm ent of conditions where there is an advantaae in lowering gastric acidity. Such conditions include duodenal and aastric ulceration, reflu>C oesophagitis and Zollinger-Ellison syndrome. Ranitidine may also be used prophylactically in surgical procedures, and in the treatment of allergic and inflammatory conditions where histamine is a known mediator.
The combination of the 5HT3 receptor antagonist of formula (I) with the H2-receptor antagonist ranitidine provides a useful and advantageous pharmaceutical preparation for the treatment of gastrointestinal disorders. A combined preparation of this type is particularly useful for the treatment of conditions such as reflux oesophagitis where the promotion of gastric emptying serves to alleviate the reflux, thereby encouraging the healing effect of the H2-receptor antagonist. Such a composition may also be useful in general anaesthesia. More particularly, when the combined preparation is given before or during anaesthesia, the promotion of gastric emptying by the 5HT3 antagonist and the reduction of gastric acid production by ranitidine prevents both acid inhalation during anaesthesia and post-anaesthetic nausea and vomitinq. The combined preparation may also be useful for the treatment of irritable bowel, syndrome.
The present invention thus provides a pharmaceutical composition, for use in human or veterinary medicine, comprising the compound of 9 t 35 3 formula (I) or a physiologically acceptable salt or solvate thereof, and ranitidine or a physiologically acceptable salt thereof.
Suitable physiologically acceptable salts of the carbazolone of formula (I) for incorporation in the composition according to the invention include acid addition salts formed with organic or inorganic acids for example, hydrochlorides, hydrobromides-, sulphates, phosphates, citrates, fumarates and maleates. The solvates may, for example, be hydrates. A preferred form of the compound of formula (I) is the hydrochloride, particularly in hydrated form, e.g. the dihydrate.
Compositions containing the compound of formula (I) in the form of a physiologically acceptable equivalent, i.e. a physiologically acceptable compound which are converted in vivo into the parent compound of formula (I), are also included within the scope of the invention.
It is preferred that ranitidine should be employed in the composition according to the invention in the form a physiologically acceptable salt. Such salts include salts of inorqanic or orqanic acids such as the hydrochloride, hydrobromide, sulphate, acetate, maleate, succinate and fumarate salts. The hydrochloride salt is particularly preferred.
A proposed dosage of the compound of formula (I) for incorporation in the pharmaceutical composition of the invention for administration to man (of approximately 70kg body weight), is 0.05 to 25m9, more preferably 0.05 to 20m9, and most preferably 0.1 to 10mg per unit dose, expressEd as the weight of free base.
The amount of ranitidine, preferably in the form a physiologically acceptable salt, employed in the pharmaceutical composition of the invention will preferably be in the range of 50-300mq.per dosage unit, expressed as the weiqht of free base.
The composition according to the invention may be administered, for example, 1 to 4 times per day. The exact dose will depend on the route of administration and the condition beinq treated, and it will be appreciated that it may be necessary to make routine variations to the dosage depending on the age and weight of the patient as well as the severity of the condition to be treated..
is The pharmaceutical compositions of the invention may be formulated in conventional manner using one or more physiologically acceptable carriers or excipients.
Thus the compositions of the invention may, for example, be formulated for oral, buccal, parenteral or rectal administration.
Particularly useful pharmaceutical compositions according to the invention are those in a form suitable for oral or rectal administration.
For oral administration, the pharmaceutical compositions may take the form of, for example, tablets or capsules prepared by conventional means with pharmaceutically acceptable excipients such as binding agents (e.g. pregelatinised maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose); fillers (e.a. lactose, microcrystalline cellulose or calcium hydroqen phosphate); lubricants (e.g. magnesium stearate, talc or silica);- disinteqrants (e.g. potato starch or sodium starch glycollate); or wetting agents (e.g. sodium lauryl sulphate). The tablets may be coated by methods well known in the art. Liquid preparations for oral administration may take the form of, for example, solutions, syrups or suspensions, or they may be presented as a dry product for constitution with water or other suitable vehicle before use. Such-liquid preparations may be prepared by conventional means with pharmaceutically acceptable additives such as suspending agents (e.g. sorbitol syrup, cellulose derivatives or hydrogenated edible fats); emulsifying agents (e.g. lecithin or acacia); non-aqueous vehicles (e.g. almond oil, oily esters, ethyl alcohol or fractionated vegetable oils);-and preservatives (e.g. methyl or propyl-p-hydroxybenzoates or sorbic acid). The preparations may also contain buffer salts, flavouring, colourinq and sweetening aaents as aopropriate.
Preparations for oral administration may be suitably formulated to give controlled release of one or both active inqredients.
For buccal administration the compositions may take the form of tablets or lozenges formulated in conventional manner.
For parenteral administration the compositions may be presented in a form Suitable for bolus injection or continuous infusion. Formulations for injection may be presented in unit dosage form e.g.
j.
f - 5 in ampoules or in multi-dose containers, with an addeo preservative. The compositions may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilising and/or dispersing agents. Alternatively, the active ingredients may be in powder form for constitution with a suitable vehicle, e.g. sterile pyrogen-free water, before use.
For rectal administration the compositions may be formulated as suppositories or retention enemas, e.q. containing conventional supppsitory,-bases such as cocoa butter or other glycerides.
Inaddition to the formulations described previously, the compositions according to the invention may also take the form of depot preparations. Such lonq-actinq formulations may be administered by implantation (for example subcutaneously or intramuscularly) or by intramuscular injection. Thus, for example, the active ingredients may be formulated with suitable polymeric or hydrophobic materials (for example as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives, for example, as a sparingly soluble salt.
The compositions may, if desired, be presented in a pack or dispenser device which may-contain one or more unit dosage forms containing the active ingredients. The pack may for examplecomprise metal or plastic foil, such as a blister pack. The pack Or dispenser device may be accompanied by instructions for administration.
The pharmaceutical compositions of the invention may be prepared according to conventional techniques well known in the pharmaceutical industry. Thus, for example, the compound of formula M or a salt or solvate thereof and the ranitidine or ranitidine salt may be admixed together, if desired, with.suitable excipients. Tablets may be prepared, for example, by direct compression of such a mixture. Capsules may be prepared by filling the blend alono with suitable excipients into gelatin capsules, usina a suitable fillina machine.. Controlled release forms for oral or rectal administration may be formulated in a conventional manner associated with controlled-release forms.
35- The followinq examples illustrate the preparation of a compound of formula (I). Temperatures are in OC.
Example 1 1y2,3,9-Tetrahydro9-methyl-3-[(2-methyl-1H-imidazol-lyl)methyll-4Hcarbazol-4-one A solution of 3-E(dimethylamino)methyll-1,2,3, 9-tetrahydro-9-methyI -4H-carbazol-4-one hydrochloride (1.7g) in water (17m1) was treated with 2-methylimidazole (1.4g) and then heated under reflux for 20h. The pooled mixture was filtered and the residue washed with water (3x15ml) to aive a product (1.7a) m.p. 221-221.50. This material was recrystallised from methanol to give the title compound (1. 4a) m.p. 231-2320.
Example 2 1,2,3,9-Tetrahydro-9-methyl-3-[(2-methyl-lH-imidazol-1yl)methyll-4Hcarbazol-4-one hydrochloride dihydrate 1,2,3,9-Tetrahydro-9methyl-3-[(2-methyl-lH-imidazol-1-yl)methyll-4Hcarbazol-4-one (18.3g) in a hot mixture of isopropanol (90ml) and water (18.3mi) was treated with concentrated hydrochloric acid (6.25ml). The hot mixture was filtered and the filtrate diluted with isopropanol (90ml) and stirred at room temperature for 17h, cooled to 20 and the solid filtered off (21.6g). A sample (6g) was recrystallized from a mixture of water (6ml) and isopropanol (10ml)-to give the title compound as a white crystalline solid (6g) m.p.
178.5-179.5 0.
Analysis Found: Cj59.45;H,6.45;N,11.5.
C18Hl9N30.HCI.2H20 requires C,59.1;H,6.6;N,11.5.1o.
V Water assay Found; 10.23,o C18Hl9N30.HCI.2H20 reauires 9.85% The followinq example illustrates a pharmaceutical composition according to the invention, containinq 1,2,3,9-tetrahydro-9-methyl-3[(2-methyl-lHimidazol-1-yl)methyll-4H-carbazol -4-one hydrochloride dihydrate (Compound A) and ranitidine hydrochloride as the active ingredients. Other physiologically acceptable salts and/or solvates of p I.
9 the compound of formula (I), and ranitidine and/or physiologically acceptable salts thereof, may be formulated in a similar manner.
TABLETS FOR ORAL ADMINISTRATION is Tablets may be prepared by the normal methods such as direct compression or wet granulation. The tablets may be film coated with suitable film forming materials, such as hydroxypropyl methylcellulose, using standard techniques.
Direct Compression Tablet Compound A, Ranitidine hydrochloride Microcrystalline cellulose NF Anhydrous lactose NF Magnesium stearate BP Compression weight Equivalent to 4.00mq free base Equivalent to 150.Omq free base Mq/tablet 5.00 168.00 100.00 75.25 1.75 350.00 Compound A and the ranitidine hydrochloride are blended with the excipients. The resultant mix is compressed into tablets usinaa suitable tablet press fitted with 9.5mm normal concave punches.
Wet Granulation Tablet Compound A Ranitidine hydrochloride Lactose BP Starch BP Pregelatinised Maize Starch BP Magnesium Stearate BP ma/tablet
10.0 112.0 130.0 30.0 15.0 3.0 (1 Compression Weight 300.0 Equivalent to 8.0mg free base.
Equivalent to 100.Omg free base -5 is The active ingrediehts are sieved through a suitable sieve and blended with lactose, starch and pregelatinised maize starch. Suitable volumes of purified water are added and the powders are granulated. After drying, the granules are screened and blended with the magnesium stearate. The granules are then compressed into tablets using 9.5mm diameter punches.
Tablets of other strengths and/or combination of doses may be prepared by appropriate alterations in the amounts of the active inqredients and the excipients and usinq punches to suit.
CAPSULES Compound A Ranitidine hydrochloride Microcrystalline Cellulose NF Magnesium Stearate BP Fill Weight ma/capsule 10.0 112.0 76.0 2.0 200.0 The active ingredients are sieved and blended with the excipients. The mix is filled into size No. 1 hard aelatin capsules using suitable machinery. Other doses may be prepared by altering the fill weight and if necessary chanaina the capsule size to suit.
SYRUP This may be either a sucrose or sucrose free c)resentation.
A.. Sucrose Syrup Comp ound A Ranitidine hydrochloride Sucrose BP Glycerine BP Buffer Flavour.) Colour Preservative) Purified Water BP to ma/5m,t dose 5.0 56.0 2750.0 500.0 as required 5.0m-t 1 The active ingredients, buffer, flavour, colour and preservative are dissolved in some of the water and the glycerine is added. The remainder of the water is heated to dissolve the sucrose and is t ' hen cooled. The two solutions are combined, adjusted to volume and mixed. The syrup is clarified by filtration.
B. Sucrose-Free ma/5mt dose Compound A 5.0 Ranitidine hydrochloride 56.0 H ydroxypropylmethylcellulose USP (viscosity type-4000) 22.5 Buffer Flavour Colour As required Preservative Sweetener Purified Water BP to 5.0mk The hydroxypropylmethylcellulose is dispersed in hot water, cooled and then mixed with an aqueous solution containing the active ingredients and the other components of the formulation. The resultant solution is adjusted to volume and mixed. The syrup is clarified by filtration.
SUPPOSITORY Compound A Ranitidine hydrochloride Witepsol H15 to 10.0mq 112.Omq 1 OCI A proprietory grade of Adeps Solidus Ph. Eur.
A suspension of the active ingredients in molten Witepsol is prepared and filled into appropriate suppository moulds using suitable machinery.
7 to
Claims (12)
1. A pharmaceutical composition for use in human or veterinary medicine comprising 1,2,3,9-tetrahydro-g-Taethyl-3 (2 -Taethyl-1H-imidazol-l-yl) methyl] -4H-carbazol-4 -one or a physiologically acceptable salt or solvate thereof and ranitidine or a physiologically acceptable salt thereof.
2. A pharmaceutical composition as claimed in claim 1 wherein 'the 1,2,3,9-tetrahydro-g-nethyl-3-[(2-methyl-1H- iTaidazol-l-yl) methyl] -4H-carbazol-4 -one is used in the form of a hydrochloride salt.
3. A pharmaceutical composition as claimed in claim 2 wherein the 1,2,3,9-tetrahydro-g-inethyl-3-[(2-methyl-1H- linidazol-l-yl) methyl] -4H-carbazol-4 -one is used in the form of the hydrochloride dihydrate.
4. A pharmaceutical composition as claimed in any of claims 1 to 3 wherein the ranitidine is used in the form of the hydrochloride salt.
5. A pharmaceutical composition as claimed in any of claims 1 to 4 in unit dose form containing 0. 05 to 25mg per unit dose of 1,2,3,9-tetrahydro-9-methyl-3-[(2-methyl-1H- imidazol-l-yl) methyl] -4H-carbazol-4 -one and 50 to 300mg per unit- dose of ranitidine, both dosages being expressed as the weight of free base.
6. A pharmaceutical composition as claimed in claim 5 in which the unit dose of 1,2,3,9-tetrahydro-g-nethyl-3-[(2- methyl-lH- imida z ol - l-yl) methyl] -4H-carbaz ol-4 -one is 0.05 to 20mg.
7. A -pharmaceutical composition as claimed in any of j 11 i Q claims 1 to 6 in a form adapted for oral, buccal, parenteral or rectal administration.
8. A pharmaceutical composition as claimed in claim 7 for oral administration in the form of tablets.
9. A pharmaceutical composition as claimed in any of claims 1 to 8 containing at least one physiologically acceptable carrier or excipient.
10. A method for the manufacture -of a pharmaceutical composition as claimed r >in any of claims 1 to 9 which 10 comprises processing the components by conventional techniques to form a pharmaceutical composition.
ll. The use of 1, 213 j 9 -tetrahydro-9 -methyl -3 - [ (2 -methyl1HiTaidazol-l-yl)methyl]-4H-carbazol-4-one or a physiologically acceptable salt or solvate thereof in a unit dose of 0.05 to 20mg, together with ranitidine or a physiologically acceptable salt thereof in a unit dose of 50 to 300mg, both doses being expressed as the weight of free base, for the manufacture of a medicament for the promotion of gastric emptying.
12. The use of 1, 2, 3, 9 -tetrahydro-g-nethyl-3 - [ (2 -methyl1H-imidaz. ol-l-yl)methyl]-4H-carbazol-4-one or a physiologically acceptable salt or solvate thereof in a unit dos e of 0.05 to 20mg, together with ranitidine or a physiologically acceptable salt thereof in a unit dose of 50 to 300mg, both doses being expressed as the weight of free base, for the manufacture of a medicament for the treatment and prevention of nausea and vomiting.
Published 1988 at The Patent.OMce. SLate House. 6571 High Holborn, London WCIR 4TP. FUrLher copies maybe obtained from The Patent =ce. Wes Branch. St Mary Cray, Orpington, Rent BR5 3RD. Printed by Multaplex teclixtiques ltd- S, Mary Cray. Kent Con. 1/87.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB858516083A GB8516083D0 (en) | 1985-06-25 | 1985-06-25 | Heterocyclic compounds |
| GB868628474A GB8628474D0 (en) | 1985-06-25 | 1986-11-28 | Pharmaceutical compositions |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| GB8727836D0 GB8727836D0 (en) | 1987-12-31 |
| GB2200046A true GB2200046A (en) | 1988-07-27 |
| GB2200046B GB2200046B (en) | 1990-09-26 |
Family
ID=40347948
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB858516083A Pending GB8516083D0 (en) | 1985-06-25 | 1985-06-25 | Heterocyclic compounds |
| GB868628474A Pending GB8628474D0 (en) | 1985-06-25 | 1986-11-28 | Pharmaceutical compositions |
| GB8727836A Expired - Fee Related GB2200046B (en) | 1985-06-25 | 1987-11-27 | Pharmaceutical compositions for treating gastric disorders |
Family Applications Before (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB858516083A Pending GB8516083D0 (en) | 1985-06-25 | 1985-06-25 | Heterocyclic compounds |
| GB868628474A Pending GB8628474D0 (en) | 1985-06-25 | 1986-11-28 | Pharmaceutical compositions |
Country Status (22)
| Country | Link |
|---|---|
| US (2) | US4753789A (en) |
| EP (2) | EP0431443A3 (en) |
| JP (2) | JPS6253920A (en) |
| AT (2) | ATE134510T1 (en) |
| AU (2) | AU609028B2 (en) |
| BE (1) | BE1002249A4 (en) |
| CA (1) | CA1296637C (en) |
| CH (1) | CH672068A5 (en) |
| CY (1) | CY2000A (en) |
| DE (2) | DE3650488T2 (en) |
| DK (1) | DK624687A (en) |
| FR (1) | FR2613934B1 (en) |
| GB (3) | GB8516083D0 (en) |
| HK (1) | HK82597A (en) |
| IE (1) | IE60908B1 (en) |
| IL (1) | IL84638A (en) |
| IT (1) | IT1211937B (en) |
| NL (1) | NL8702853A (en) |
| NZ (1) | NZ222743A (en) |
| SE (1) | SE8704747L (en) |
| SG (1) | SG43311A1 (en) |
| ZA (1) | ZA878927B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT401727B (en) * | 1989-02-23 | 1996-11-25 | Glaxo Canada | GELATINE CAPSULES CONTAINING RANITIDINE (SALT) |
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| DE3688296T2 (en) * | 1985-03-14 | 1993-11-04 | Beecham Group Plc | MEDICINES FOR TREATING EMERGENCY. |
| GB8516083D0 (en) * | 1985-06-25 | 1985-07-31 | Glaxo Group Ltd | Heterocyclic compounds |
| US5578628A (en) * | 1985-06-25 | 1996-11-26 | Glaxo Group Limited | Medicaments for the treatment of nausea and vomiting |
| GB8627909D0 (en) * | 1986-11-21 | 1986-12-31 | Glaxo Group Ltd | Medicaments |
| US4845115A (en) * | 1986-12-17 | 1989-07-04 | Glaxo Group Limited | Method of medical treatment |
| US5330982A (en) * | 1986-12-17 | 1994-07-19 | Glaxo Group Limited | Pharmaceutical composition containing a 5-HT receptor antagonist and an H+ K+ Atpase inhibitor and a method of treating gastrointestingal disorders therewith |
| GB8630080D0 (en) * | 1986-12-17 | 1987-01-28 | Glaxo Group Ltd | Medicaments |
| GB8630071D0 (en) * | 1986-12-17 | 1987-01-28 | Glaxo Group Ltd | Medicaments |
| GB8630079D0 (en) * | 1986-12-17 | 1987-01-28 | Glaxo Group Ltd | Medicaments |
| JPH0754759B2 (en) * | 1987-04-27 | 1995-06-07 | 日本電信電話株式会社 | Plasma processing method and apparatus, and mode converter for plasma processing apparatus |
| US4943428A (en) * | 1987-07-10 | 1990-07-24 | Wright State University | Stimulation of serotonin-1A receptors in mammals to alleviate motion sickness and emesis induced by chemical agents |
| DE3822792C2 (en) * | 1987-07-11 | 1997-11-27 | Sandoz Ag | New use of 5HT¶3¶ antagonists |
| GB8805269D0 (en) * | 1988-03-04 | 1988-04-07 | Glaxo Group Ltd | Medicaments |
| GB8806224D0 (en) * | 1988-03-16 | 1988-04-13 | Johnson Matthey Plc | Platinum chemotherapeutic product |
| GB8816187D0 (en) * | 1988-07-07 | 1988-08-10 | Glaxo Group Ltd | Medicaments |
| US5047246A (en) * | 1988-09-09 | 1991-09-10 | Bristol-Myers Company | Direct compression cyclophosphamide tablet |
| AU627221B2 (en) * | 1988-09-27 | 1992-08-20 | Fujisawa Pharmaceutical Co., Ltd. | Pyridoindole derivatives and processes for preparation thereof |
| US5039528A (en) * | 1989-12-11 | 1991-08-13 | Olney John W | EAA antagonists as anti-emetic drugs |
| US4971651A (en) * | 1990-02-05 | 1990-11-20 | Hitachi, Ltd. | Microwave plasma processing method and apparatus |
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| EP0591434A4 (en) * | 1991-06-26 | 1994-09-14 | Sepracor Inc | Method and compositions for treating emesis, nausea and other disorders using optically pure r(+) ondansetron |
| EP1082959A1 (en) * | 1991-09-20 | 2001-03-14 | Glaxo Group Limited | NK1 Antagonists for the treatment of depression |
| WO1994020102A2 (en) * | 1993-03-08 | 1994-09-15 | Fujisawa Pharmaceutical Co., Ltd. | Medicament for treating or preventing cerebrovascular diseases |
| GB9423511D0 (en) * | 1994-11-22 | 1995-01-11 | Glaxo Wellcome Inc | Compositions |
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| JP2010050046A (en) | 2008-08-25 | 2010-03-04 | Hitachi High-Technologies Corp | Plasma treatment device |
| CA2784587A1 (en) | 2009-12-28 | 2011-07-28 | Monosol Rx, Llc | Orally administrable film dosage forms containing ondansetron |
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Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0201165A2 (en) * | 1985-03-14 | 1986-11-12 | Beecham Group Plc | Medicaments for the treatment of emesis |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0040489A1 (en) * | 1980-05-17 | 1981-11-25 | FISONS plc | Mixtures, salts, packages and pharmaceutical compositions containing 5-(2-hydroxypropoxy)-4-oxo-8-propyl-4H-1-benzopyran-2-carboxylic acid or a derivative thereof and an H2 receptor antagonist antihistamine |
| BE894285A (en) * | 1981-09-04 | 1983-03-02 | Glaxo Group Ltd | PHARMACEUTICAL COMPOSITION CONTAINING AN ANTI-INFLAMMATORY MEDICINAL PRODUCT AND RANITIDINE OR A SALT THEREOF |
| FR2557110B1 (en) * | 1983-12-23 | 1989-11-24 | Sandoz Sa | NOVEL CYCLIC AMINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS MEDICAMENTS |
| IT1182150B (en) * | 1984-01-25 | 1987-09-30 | Glaxo Group Ltd | TETRAIDROCARBOZOLONICI HETEROCYCLIC COMPOUNDS, PROCEDURES FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
| US4695578A (en) * | 1984-01-25 | 1987-09-22 | Glaxo Group Limited | 1,2,3,9-tetrahydro-3-imidazol-1-ylmethyl-4H-carbazol-4-ones, composition containing them, and method of using them to treat neuronal 5HT function disturbances |
| AU583343B2 (en) * | 1985-01-23 | 1989-04-27 | Glaxo Group Limited | Heterocyclic compounds |
| GB8516083D0 (en) * | 1985-06-25 | 1985-07-31 | Glaxo Group Ltd | Heterocyclic compounds |
| GB8630079D0 (en) * | 1986-12-17 | 1987-01-28 | Glaxo Group Ltd | Medicaments |
-
1985
- 1985-06-25 GB GB858516083A patent/GB8516083D0/en active Pending
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1986
- 1986-06-24 DE DE3650488T patent/DE3650488T2/en not_active Expired - Lifetime
- 1986-06-24 EP EP19900122615 patent/EP0431443A3/en not_active Withdrawn
- 1986-06-24 US US06/877,805 patent/US4753789A/en not_active Expired - Lifetime
- 1986-06-24 JP JP61147996A patent/JPS6253920A/en active Granted
- 1986-06-24 SG SG1996008047A patent/SG43311A1/en unknown
- 1986-06-24 AT AT86304831T patent/ATE134510T1/en not_active IP Right Cessation
- 1986-06-24 EP EP86304831A patent/EP0226266B1/en not_active Expired - Lifetime
- 1986-11-28 GB GB868628474A patent/GB8628474D0/en active Pending
- 1986-12-30 AU AU67037/86A patent/AU609028B2/en not_active Expired
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1987
- 1987-11-27 BE BE8701354A patent/BE1002249A4/en not_active IP Right Cessation
- 1987-11-27 AT AT0312587A patent/AT395374B/en not_active IP Right Cessation
- 1987-11-27 IT IT8748643A patent/IT1211937B/en active
- 1987-11-27 DK DK624687A patent/DK624687A/en not_active Application Discontinuation
- 1987-11-27 NL NL8702853A patent/NL8702853A/en not_active Application Discontinuation
- 1987-11-27 CA CA000552962A patent/CA1296637C/en not_active Expired - Fee Related
- 1987-11-27 CH CH4613/87A patent/CH672068A5/fr not_active IP Right Cessation
- 1987-11-27 IL IL84638A patent/IL84638A/en not_active IP Right Cessation
- 1987-11-27 DE DE19873740351 patent/DE3740351A1/en not_active Withdrawn
- 1987-11-27 ZA ZA878927A patent/ZA878927B/en unknown
- 1987-11-27 IE IE323087A patent/IE60908B1/en not_active IP Right Cessation
- 1987-11-27 JP JP62299653A patent/JPS63198623A/en active Pending
- 1987-11-27 GB GB8727836A patent/GB2200046B/en not_active Expired - Fee Related
- 1987-11-27 SE SE8704747A patent/SE8704747L/en not_active Application Discontinuation
- 1987-11-27 FR FR8716489A patent/FR2613934B1/en not_active Expired - Fee Related
- 1987-11-30 AU AU81914/87A patent/AU616386B2/en not_active Ceased
- 1987-11-30 NZ NZ222743A patent/NZ222743A/en unknown
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1988
- 1988-04-04 US US07/177,042 patent/US4929632A/en not_active Expired - Lifetime
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1997
- 1997-06-19 HK HK82597A patent/HK82597A/en not_active IP Right Cessation
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Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0201165A2 (en) * | 1985-03-14 | 1986-11-12 | Beecham Group Plc | Medicaments for the treatment of emesis |
Non-Patent Citations (1)
| Title |
|---|
| MARTINDALE, THE EXTRA PHARMACOPOEIA, 28TH EDITION (1982). PAGES 1318-19 SEE ENTRY. 6162-E * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT401727B (en) * | 1989-02-23 | 1996-11-25 | Glaxo Canada | GELATINE CAPSULES CONTAINING RANITIDINE (SALT) |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20041127 |