NZ283354A - Oral pharmaceutical comprising low dosage amount of ranitidine as sole active ingredient for treating minor gastrointestinal disorders associated with excess acid secretion - Google Patents
Oral pharmaceutical comprising low dosage amount of ranitidine as sole active ingredient for treating minor gastrointestinal disorders associated with excess acid secretionInfo
- Publication number
- NZ283354A NZ283354A NZ283354A NZ28335495A NZ283354A NZ 283354 A NZ283354 A NZ 283354A NZ 283354 A NZ283354 A NZ 283354A NZ 28335495 A NZ28335495 A NZ 28335495A NZ 283354 A NZ283354 A NZ 283354A
- Authority
- NZ
- New Zealand
- Prior art keywords
- ranitidine
- oral pharmaceutical
- pharmaceutical composition
- tablet
- disorders associated
- Prior art date
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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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
-
- 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
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Description
<div class="application article clearfix" id="description">
<p class="printTableText" lang="en">New Zealand Paient Spedficaiion for Paient Number £83354 <br><br>
New Zealand No. 283354 International No. PCT/EP95/01271 <br><br>
TO BE ENTERED AFTER ACCEPTANCE AND PUBLICATION <br><br>
Priority dates: 12.04.1994; <br><br>
Complete Specification Filed: 10.04.1995 <br><br>
Classification:^) A61K31/34 <br><br>
Publication date: 26 August 1998 <br><br>
Journal No.: 1431 <br><br>
Title of Invention: <br><br>
Low dosage ranitidine compositions for the treatment of minor gastrointestinal disorders associated with excess acid secretion <br><br>
Name, address and nationality of applicant(s) as in international application form: <br><br>
GLAXO GROUP LIMITED, Glaxo Wellcome House, Berkeley Avenue, Greenford, Middx, UB6 ON'N, Great Britain <br><br>
NEW ZEALAND PATENTS ACT 1953 <br><br>
COMPLETE SPECIFICATION <br><br>
WO 95/27486 <br><br>
PCTAEP95/01271 <br><br>
283354 <br><br>
LOW DOSAGE RANITIDINE COMPOSITIONS FOR THE TREATMENT OF MINOR GASTROINTESTINAL DISORDERS ASSOCIATED WITH EXCESS ACID SECRETION <br><br>
The present invention relates to low dosage formulations containing the histamine Hz-receptor antagonist ranitidine and their use in the treatment of 5 gastric disorders such as episodic heartburn. <br><br>
Ranitidine, N-[2-[[[5-(dimethylamino)methyl-2-furanyl]methyI]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine, and its physiologically acceptable salts are described and claimed in British Patent Specification No. 1565966, and a 10 particular crystalline form of ranitidine hydrochloride is described and claimed in British Patent Specification No. 2084580. In both these specifications there is reference to formulations for oral administration, which may take the form of for example tablets, capsules, granules, powders, solutions, syrups, suspensions, or tablets or lozenges for buccal administration. Oral administration constitutes 15 a preferred route for administering ranitidine. <br><br>
US Patent No. 5229137 describes the use of a combination of ranitidine and an antacid for the treatment of episodic heartburn. According to US 5229137, when H2-antagonists such as ranitidine are administered alone, relief from 20 episodic heartburn is not experienced until some time after the medication is ingested. Specifically, when 150mg of ranitidine were administered to two patients suffering from episodic heartburn, relief was obtained 45 and 60 minutes after ingestion. Therefore, according to US 5229137, an antacid needs to be administered with the Hr-antagonist in order to obtain rapid relief. When 25 the Hr-antagonist is ranitidine, the doses used in the combination are between 100 and 150mg. <br><br>
Compositions containing reduced doses of Hr-antagonists are described in EP0193400 and W093/12779. EP0193400 describes a combination of an 30 H2.antagonist, such as ranitidine, and sodium polyacrylate for use in the treatment of gastritis or gastro-duodenal ulcers. According to EP0193400, the synergistic effect between the H2-antagonist and polyacrylate affords the possibility of the lower doses of H2-antagonist being used. <br><br>
WO 95/27486 <br><br>
PCT /EP95/01271 <br><br>
2 <br><br>
W093/12779 describes the use of a combination of an H^ntagonist, including ranitidine, and an antacid in the treatment of gastric disorders, where the combination is buffered to confer a pH substantially equal to that of the pKa of the ^antagonist and where the dose of the Hr-antagonist per unit dosage form is less than 25mg. The lower dose is said to be effective since the combination of active agents increases bioavailability of the Hr-antagonist at the local stomach wall receptor site. <br><br>
EP0492247 also describes a composition having a reduced dose of H2.antagonist for the treatment of heartburn etc. Here the composition uses a combination of water-soluble H2-antagonist and an effervescent delivery system, such as an alkali metal bicarbonate and citric acid. The use of the effervescent delivery system is said to decrease the time for onset of action of the H2.antagonist and increases its potency such that the formulation requires about twenty-five per cent of the Hz-antagonist dosage currently prescribed for the treatment of active duodenal ulcer. In the case of ranitidine, the effervescent delivery system reduces the dosage from 150mg to less than about 37.5mg. <br><br>
Dosage levels between 50 and 600mg, such as 150 and 300mg, of ranitidine when administered alone are conventionally regarded as conferring therapeutic benefit. <br><br>
Surprisingly, it has now been found that very low doses of ranitidine, administered alone, are effective in the treatment of minor gastrointestinal disorders associated with excess acid secretion, such as episodic heartburn for example, and that relief from symptoms occurs within 30-45 minutes after ingestion. Duration of control of acid secretion is also advantageous with the dosage of the invention. <br><br>
Thus, the present invention provides an oral pharmaceutical composition, such as a tablet, comprising ranitidine, or a physiologically acceptable salt thereof, as the sole active ingredient, characterised in that the dose of ranitidine per unit dosage form is between 10 and 30mg, such as 25mg, expressed as the weight of free base. <br><br>
1257HA/C <br><br>
% <br><br>
283354 <br><br>
According to a further aspect the present invention provides a swallow tablet comprising ranitidine, or a physiologically acceptable salt thereof, as the sole active ingredient, characterised in that the dose of ranitidine per unit dosage form is between 10 and 30mg, such as 25mg, expressed as the weight of free 5 base. <br><br>
According to a further aspect the present invention provides the use of an oral pharmaceutical composition comprising ranitidine, or a physiologically acceptable salt thereof, as the sole active ingredient, in the manufacture of a medicament 10 for treating minor gastrointestinal disorders associated with excess acid secretion, characterised in that the dose of ranitidine per unit dosage form is between 10 and 30mg, such as 25mg, expressed as the weight of free base. <br><br>
15 It will be understood that the compositions according to Hie invention are . substantially free from antacids, a polyacrylate or an effervescent delivery system. <br><br>
Ranitidine may be employed in the tablets according to the invention in the form 20 of either its free base or a physiologically acceptable salt Such salts include salts with inorganic or organic acids such as the hydrochloride, hydrobromide, sulphate, acetate, maleate, succinate, citrate, tartrate, fumarate and ascorbate salts. A particularly preferred salt of ranitidine is the hydrochloride. <br><br>
25 Ranitidine may be employed in the tablets according to the invention in conventional form or coated or encapsulated forms of ranitidine may be used. Suitable coated and encapsulated forms are described in, for example, EP538034, EP523847, W092/21328, EP473431, EP459695, EP349103, CA2068366 and US5084278. Ranitidine resin adsorbates as described in 30 UK2218333 may also be incorporated into the tablets according to the present invention. <br><br>
Preferably ranitidine and its salts are used in conventional form. <br><br>
INTELLECTUAL PROPERTY OFFICE OF N.Z. <br><br>
i: ys.\ 'u3 <br><br>
RECEIVED <br><br>
t <br><br>
25 <br><br>
30 <br><br>
WO 95/27486 PCT/EP95/01271 <br><br>
4 <br><br>
The amount of ranitidine, preferably in the form of a physiologically acceptable salt, particularly ranitidine hydrochloride, in the composition according to the invention is preferably in the range of 10 to 30mg per dosage unit (for example per tablet), e.g. 25mg, expressed as the weight of free base. <br><br>
The unit dose (for example contained in one tablet according to the invention) may be administered up to, for example, 12 times a day depending upon the nature and severity of the conditions being treated, and the age and weight of the patient. Thus, for example, in the treatment of minor gastrointestinal disorders associated with excess acid secretion such as, for example, acid indigestion, over-indulgence of food or drink (e.g. alcoholic beverages), acid stomach, sour stomach, waterbrash/regurgitation, heartburn, such as episodic heartburn, nocturnal heartburn, and meal-induced heartburn, gastritis and dyspepsia, a 10-30mg dose of ranitidine, e.g. a 25mg dose, expressed as the weight of free base, may be administered up to 12 times a day, for example 6 times a day, as and when required. <br><br>
The pharmaceutical compositions according to the invention may also contain other excipients conventional to the art such as fillers, binders, disintegrants, lubricants and dessicants. Suitable excipients are well-known to those skilled in the art. <br><br>
Suitable binders include methylcellulose, sodium carboxymethylcellulose, hydroxypropyl methylcellulose, alginic acid, ethylceliulose, acacia, gelatin, pregelatinised starch, sucrose syrup, polyvinylpyrrolidone (povidone) and guar gum. <br><br>
Suitable lubricants include magnesium stearate, zinc stearate, calcium stearate, stearic acid, sodium stearyl fumarate, hydrogenated vegetable oils, glyceryl palmitostearate, glyceryl behenate, sodium benzoate, sodium lauryl sulphate, magnesium lauryl sulphate, mineral oil, talc and mixtures thereof. <br><br>
Magnesium stearate is a preferred lubricant. <br><br>
Suitable dessicants include silica gel. <br><br>
WO 95/27486 <br><br>
PCT/EP95/01271 <br><br>
5 <br><br>
Suitable fillers include microcrysalline cellulose. Suitable disintegrants include croscarmellose sodium. <br><br>
Suitable chewable tablets are described in our co-pending PCT Application No. PCT/EP93/02763. Chewable tablets specifically disclosed in this co-pending application are not included within the scope of the present invention. <br><br>
Such chewable tablets comprise ranitidine, or a physiologically acceptable salt thereof, a chewable base selected from sucrose, glucose, lactose, maltose, or a mixture thereof, a flavouring and, optionally an intense sweetener. <br><br>
The chewable tablets may be prepared using the conventional stages of mixing, granulation, drying, blending, compression and packing. <br><br>
Suitable swallow tablet cores may be prepared in a conventional manner, for example in a similar manner to that described in British Patent Specification No. 2084580 which is incorporated herein by reference. Thus, for example the required quantities of ranitidine or its salt, a lubricant, such as magnesium stearate and optionally a pharmaceutically acceptable disintegrant, such as croscarmellose sodium, are mixed and compressed into tablet cores. <br><br>
Swallow tablets are conventionally film-coated according to conventional procedures either by aqueous or organic techniques. A preferred film coat is described in British Patent specification No. 2218336 which is incorporated herein by reference. <br><br>
The following are illustrations of non-limiting examples of the pharmaceutical compositions according to the invention. Opaspray white K-1-7000 is a suspension of titanium dioxide and hydroxypropyl cellulose in industrial methylated spirits. Opadry Yellow Y S-1-12606 is a mixture of hydroxypropyl methylcellulose 2910, titanium dioxide, triacetin and iron oxide yellow. Both Opaspray and Opadry are the tradenames of Colorcon Inc., West Point, Philadelphia, USA. <br><br>
WO 95/27486 <br><br>
PCT/EP95/01271 <br><br>
6 <br><br>
Reference Example 1 Chewable Tablet <br><br>
Ingredient <br><br>
Ranitidine HCI Sucrose Aspartame Povidone <br><br>
Peppermint Flavour Silica Gel <br><br>
Magnesium Stearate Isopropyl Alcohol + <br><br>
+ not present in final product <br><br>
Example 2 Swallow Tablet <br><br>
Tablet Core mg/tat'^t <br><br>
Ranitidine HCI 28.0 <br><br>
Macrocrystalline Cellulose 263.75 <br><br>
Croscarmellose Sodium Type A 6.00 <br><br>
Magnesium Stearate 2.25 <br><br>
Target compression weight 300mg <br><br>
Film Coat % w/w Unit amounts <br><br>
(mg/tablet)* <br><br>
Methylhydroxypropyl Cellulose 4.0 11.3 <br><br>
Opaspray White K-1-7000 3.3 4.7 <br><br>
Isopropyl Alcohol ** 26.3 qs <br><br>
Dichloromethane ** 66.4 qs nig/tablet <br><br>
28.0 2268.0 37.5 50.0 41.5 50.0 25.0 qs <br><br></p>
</div>
Claims (7)
1. Use of an oral pharmaceutical composition comprising ranitidine, or a physiologically acceptable salt thereof, as the sole active ingredient, in the manufacture of a medicament for treating minor gastrointestinal disorders associated with excess acid secretion, characterised in that the dose of ranitidine per unit dosage form is between 10 and 30 mg, expressed as the weight of free base.<br><br>
2. Use of an oral pharmaceutical composition as claimed in claim 1 where the dose of ranitidine per dosage unit is 25mg expressed as the weight of free base.<br><br>
3. Use of an oral pharmaceutical composition as claimed in claim 1 or claim 2 where the ranitidine is in the form of its hydrochloride salt.<br><br>
4. Use of an oral pharmaceutical composition as claimed in any one of claims 1 to 3 in the form of a tablet.<br><br>
5. Use of an oral pharmaceutical composition as claimed in claim 4 in the form of a swallow tablet.<br><br>
6. Use of an oral pharmaceutical composition as defined in claim 1 substantially as herein described with reference to any example thereof.<br><br>
7. Use as claimed in claim 1 of an oral pharmaceutical composition in the manufacture of a medicament substantially as herein described with reference to any example thereof.<br><br> -S OF CLAIMS<br><br> </p> </div>
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9407235A GB9407235D0 (en) | 1994-04-12 | 1994-04-12 | Pharmaceutical compositions |
PCT/EP1995/001271 WO1995027486A1 (en) | 1994-04-12 | 1995-04-10 | Low dosage ranitidine compositions for the treatment of minor gastrointestinal disorders associated with excess acid secretion |
Publications (1)
Publication Number | Publication Date |
---|---|
NZ283354A true NZ283354A (en) | 1998-08-26 |
Family
ID=10753423
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NZ283354A NZ283354A (en) | 1994-04-12 | 1995-04-10 | Oral pharmaceutical comprising low dosage amount of ranitidine as sole active ingredient for treating minor gastrointestinal disorders associated with excess acid secretion |
Country Status (11)
Country | Link |
---|---|
EP (1) | EP0755251A1 (en) |
JP (1) | JPH10502331A (en) |
KR (1) | KR970702034A (en) |
CN (1) | CN1146150A (en) |
AU (1) | AU690664B2 (en) |
BR (1) | BR9507312A (en) |
CA (1) | CA2187651A1 (en) |
GB (1) | GB9407235D0 (en) |
NZ (1) | NZ283354A (en) |
WO (1) | WO1995027486A1 (en) |
ZA (1) | ZA952931B (en) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9025710D0 (en) * | 1990-11-27 | 1991-01-09 | Beecham Group Plc | Novel treatment |
CA2055661A1 (en) * | 1990-12-21 | 1992-06-22 | Manley A. Paulos | Treatment of upset stomach associated with heartburn, sour stomach or acid indigestion with an effervescent h2 blocker formulation |
GB9127150D0 (en) * | 1991-12-20 | 1992-02-19 | Smithkline Beecham Plc | Novel treatment |
-
1994
- 1994-04-12 GB GB9407235A patent/GB9407235D0/en active Pending
-
1995
- 1995-04-10 CN CN95192537A patent/CN1146150A/en active Pending
- 1995-04-10 AU AU21380/95A patent/AU690664B2/en not_active Ceased
- 1995-04-10 EP EP95914346A patent/EP0755251A1/en not_active Withdrawn
- 1995-04-10 BR BR9507312A patent/BR9507312A/en unknown
- 1995-04-10 JP JP7526068A patent/JPH10502331A/en active Pending
- 1995-04-10 NZ NZ283354A patent/NZ283354A/en unknown
- 1995-04-10 WO PCT/EP1995/001271 patent/WO1995027486A1/en not_active Application Discontinuation
- 1995-04-10 CA CA002187651A patent/CA2187651A1/en not_active Abandoned
- 1995-04-10 ZA ZA952931A patent/ZA952931B/en unknown
-
1996
- 1996-10-11 KR KR1019960705716A patent/KR970702034A/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
BR9507312A (en) | 1997-10-07 |
WO1995027486A1 (en) | 1995-10-19 |
AU2138095A (en) | 1995-10-30 |
EP0755251A1 (en) | 1997-01-29 |
CA2187651A1 (en) | 1995-10-19 |
JPH10502331A (en) | 1998-03-03 |
AU690664B2 (en) | 1998-04-30 |
KR970702034A (en) | 1997-05-13 |
ZA952931B (en) | 1996-01-05 |
GB9407235D0 (en) | 1994-06-08 |
MX9604553A (en) | 1997-11-29 |
CN1146150A (en) | 1997-03-26 |
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