WO1997025065A1 - Oral pharmaceutical dosage forms comprising a proton pump inhibitor and a prokinetic agent - Google Patents
Oral pharmaceutical dosage forms comprising a proton pump inhibitor and a prokinetic agent Download PDFInfo
- Publication number
- WO1997025065A1 WO1997025065A1 PCT/SE1996/001736 SE9601736W WO9725065A1 WO 1997025065 A1 WO1997025065 A1 WO 1997025065A1 SE 9601736 W SE9601736 W SE 9601736W WO 9725065 A1 WO9725065 A1 WO 9725065A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- dosage form
- enteric coating
- proton pump
- pump inhibitor
- tablet
- 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.)
- Ceased
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- 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
Definitions
- the present invention is related to new oral pharmaceutical preparations especially for use in the prevention and treatment of disorders associated with gastro oesophageal reflux.
- the present preparations comprise a gastric acid suppressing agent, such as a proton pump inhibitor, in combination with one or more prokinetic agents in a new fixed unit dosage form, especially a tablet
- the present invention refers to a method for the manufacture of such preparations and the use of such preparations in medicine, especially in the treatment of gastro oesophageal reflux diseases and other gastrointestinal disorders.
- Antacids and alginates are still widely used. They have a short duration of action but are seen as inexpensive and safe. They do not provide a layterm symptom resolution of GORD.
- the gastric acid suppressing agent is preferably an acid susceptible proton pump inhibitor but other gastric acid suppressing agents such as the H 2 receptor antagonists: ranitidine, cimetidine or famotidine, may be used together with a prokinetic agent in the pharmaceutical compositions according to the present invention.
- gastric acid suppressing agents such as the H 2 receptor antagonists: ranitidine, cimetidine or famotidine, may be used together with a prokinetic agent in the pharmaceutical compositions according to the present invention.
- the seeds which are to be layered with the proton pump inhibitor can be water insoluble seeds comprising different oxides, celluloses, organic polymers and other materials, alone or in mixtures or water-soluble seeds comprising different inorganic salts, sugars, non-pareils and other materials, alone or in mixtures. Further, the seeds may comprise the proton pump inhibitor in the form of crystals, agglomerates, compacts etc. The size of the seeds is not essential for the present invention but may vary between approximately 0.1 and 2 mm.
- the seeds layered with the proton pump inhibitor are produced either by powder or solution/suspension layering using for instance granulation or spray coating layering equipment
- Pellets covered with enteric coating layer(s) may further be covered with one or more over ⁇ coating layer(s).
- the over-coating layer(s) should be water soluble or rapidly disintegrating in water.
- the over-coating layer(s) can be applied to the enteric coating layered pellets by coating or layering procedures in suitable equipments such as coating pan, coating granulator or in a fluidized bed apparatus using water and/or organic solvents for the coating or layering process.
- the active substance(s) in form of one or more prokinetic compound(s) is dry mixed with inactive excipients and the mixture is wet massed with a granulation liquid.
- the wet mass is dried preferably to a loss on drying of less than 3% by weight. Thereafter the dry mass is milled to a suitable size for the granules, such as smaller than 4 mm, and preferably smaller than 1 mm.
- suitable inactive excipients for the prokinetic mixture are for instance lactose, corn starch low substituted hydroxypropyl cellulose, microcrystalline cellulose, sodium starch glycolate and crosslinked polyvinyl pyrrolidone.
- Suitable lubricants for the tableting process are for instance sodium stearyl fumarate, magnesium stearate and talc.
- Multiple unit dosage form comprising magnesium omeprazole and mosapride (batch size 500 tablets).
- Suspension layering was performed in a fluid bed apparatus. Lansoprazole was sprayed onto the sugar sphere seeds from a suspension containing the dissolved binder in a water solution. Pellets covered with separating layer and enteric coating layer were produced as in example 1.
- a capsule formulation comprising magnesium omeprazole and mosapride (batch size 100 capsules).
- Multiple unit dosage form comprising magnesium omeprazole with a tablet coating layer comprising mosapride (batch size 1 000 tablets).
- Polyethylene glycol 6000 75 g Mono- and diglycerides (NF) 12.5 g
Landscapes
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (18)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MX9706769A MX9706769A (es) | 1996-01-08 | 1996-12-20 | Formas de dosificacion farmaceutica que comprenden un inhibidor de la bomba de protones y un agente procinetico. |
| IL12165296A IL121652A (en) | 1996-01-08 | 1996-12-20 | Pharmaceutical dosage forms for oral administration that include a proton pump inhibitor and a prokinetic substance |
| US08/750,936 US6132771A (en) | 1996-01-08 | 1996-12-20 | Oral pharmaceutical dosage forms comprising a proton pump inhibitor and a prokinetic agent |
| PL96322176A PL322176A1 (en) | 1996-01-08 | 1996-12-20 | Oral pharmaceutic administration forms containing the protonic pump inhibitor and a prokinetic agent |
| AT96944725T ATE228010T1 (de) | 1996-01-08 | 1996-12-20 | Orale pharmazeutische dosierungsformen die einen protonenpumpeninhibitor und ein prokinetisches mittel enthalten |
| NZ325976A NZ325976A (en) | 1996-01-08 | 1996-12-20 | Compositions comprising an enteric coated acid susceptible proton pump inhibitor and a prokinetic agent |
| AU13240/97A AU712572B2 (en) | 1996-01-08 | 1996-12-20 | Oral pharmaceutical dosage forms comprising a proton pump inhibitor and a prokinetic agent |
| JP9525130A JPH11501949A (ja) | 1996-01-08 | 1996-12-20 | プロトンポンプ抑制剤およびプロキネティック剤を含有する経口用医薬剤形 |
| DK96944725T DK0814840T3 (da) | 1996-01-08 | 1996-12-20 | Orale farmaceutiske doseringsformer, der omfatter en protonpumpeinhibitor og et prokinetisk middel |
| CA002214033A CA2214033C (en) | 1996-01-08 | 1996-12-20 | Oral pharmaceutical dosage forms comprising a proton pump inhibitor and a prokinetic agent |
| SK1170-97A SK117097A3 (en) | 1996-01-08 | 1996-12-20 | Oral pharmaceutical dosage forms comprising a proton pump inhibitor and a prokinetic agent |
| EE9700195A EE9700195A (et) | 1996-01-08 | 1996-12-20 | Peroraalne farmatseutiline annusvorm, mis sisaldab prootonpumba inhibiitorit ja prokineetilist ainet |
| HU9904094A HUP9904094A3 (en) | 1996-01-08 | 1996-12-20 | Oral pharmaceutical dosage forms comprising a proton pump inhibitor and a prokinetic agent |
| BR9607344A BR9607344A (pt) | 1996-01-08 | 1996-12-20 | Formas de dosagem farmacéutica oral e de tablete processos para preparar a forma de dosagem fixada e para tratar distúrbios associados ás doenças de refluxo gastro-esofrágico e uso da forma de dosagem |
| DE69624910T DE69624910T2 (de) | 1996-01-08 | 1996-12-20 | Orale pharmazeutische dosierungsformen die einen protonenpumpeninhibitor und ein prokinetisches mittel enthalten |
| EP96944725A EP0814840B1 (en) | 1996-01-08 | 1996-12-20 | Oral pharmaceutical dosage forms comprising a proton pump inhibitor and a prokinetic agent |
| IS4550A IS4550A (is) | 1996-01-08 | 1997-08-21 | Lyf í formi skammta til inntöku um munn sem inniheldur prótónupumpublokkara og prókínetískt efni |
| NO19974070A NO316425B1 (no) | 1996-01-08 | 1997-09-04 | Orale, farmasöytiske doseringsformer innbefattende en protonpumpeinhibitorog et prokinetisk middel, fremgangsmåte for fremstilling av slikedoseringsformer og anvendelse derav |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9600072A SE9600072D0 (sv) | 1996-01-08 | 1996-01-08 | New oral formulation of two active ingredients II |
| SE9600072-4 | 1996-01-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1997025065A1 true WO1997025065A1 (en) | 1997-07-17 |
Family
ID=20400970
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/SE1996/001736 Ceased WO1997025065A1 (en) | 1996-01-08 | 1996-12-20 | Oral pharmaceutical dosage forms comprising a proton pump inhibitor and a prokinetic agent |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US6132771A (https=) |
| EP (1) | EP0814840B1 (https=) |
| JP (1) | JPH11501949A (https=) |
| KR (1) | KR100486057B1 (https=) |
| CN (1) | CN1142792C (https=) |
| AR (1) | AR008750A1 (https=) |
| AT (1) | ATE228010T1 (https=) |
| AU (1) | AU712572B2 (https=) |
| BR (1) | BR9607344A (https=) |
| CA (1) | CA2214033C (https=) |
| CZ (1) | CZ280897A3 (https=) |
| DE (1) | DE69624910T2 (https=) |
| DK (1) | DK0814840T3 (https=) |
| EE (1) | EE9700195A (https=) |
| ES (1) | ES2185816T3 (https=) |
| HU (1) | HUP9904094A3 (https=) |
| ID (1) | ID18383A (https=) |
| IL (1) | IL121652A (https=) |
| IS (1) | IS4550A (https=) |
| MX (1) | MX9706769A (https=) |
| NO (1) | NO316425B1 (https=) |
| NZ (1) | NZ325976A (https=) |
| PL (1) | PL322176A1 (https=) |
| PT (1) | PT814840E (https=) |
| SE (1) | SE9600072D0 (https=) |
| SK (1) | SK117097A3 (https=) |
| TR (1) | TR199700917T1 (https=) |
| WO (1) | WO1997025065A1 (https=) |
| ZA (1) | ZA9610938B (https=) |
Cited By (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999048498A1 (en) * | 1998-03-20 | 1999-09-30 | A/S Gea Farmaceutisk Fabrik | Pharmaceutical formulation comprising a 2- [[(2- pyridinyl) methyl] sulfinyl] benzimidazole having anti-ulcer activity and a process for the preparation of such formulation |
| US6132771A (en) * | 1996-01-08 | 2000-10-17 | Astrazeneca Ab | Oral pharmaceutical dosage forms comprising a proton pump inhibitor and a prokinetic agent |
| JP2001525366A (ja) * | 1997-12-08 | 2001-12-11 | ビイク グルデン ロンベルク ヒエーミツシエ フアブリーク ゲゼルシヤフト ミツト ベシユレンクテル ハフツング | 酸不安定な活性化合物を含有する新規の投与形 |
| WO2004035090A1 (en) * | 2002-10-16 | 2004-04-29 | Orexo Ab | Gastric acid secretion inhibiting composition |
| US6780882B2 (en) | 1996-01-04 | 2004-08-24 | The Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and method of using same |
| US6780435B2 (en) | 1997-11-14 | 2004-08-24 | Andrx Pharmaceuticals, Inc. | Omeprazole formulation |
| WO2004071374A3 (en) * | 2003-02-11 | 2004-12-16 | Torrent Pharmaceuticals Ltd | Once a day orally administered pharmaceutical compositions |
| EP1173067A4 (en) * | 1999-04-01 | 2005-11-09 | Wrigley W M Jun Co | STRUCTURES WITH LONG-LASTING FLAVOR FOR CHEESE |
| US7070805B2 (en) | 1998-07-28 | 2006-07-04 | Takeda Pharmaceutical Company Limited | Rapidly disintegrable solid preparation |
| US7404968B2 (en) * | 1999-08-18 | 2008-07-29 | Microdose Technologies, Inc. | Metering and packaging of controlled release medication |
| US7431942B2 (en) | 1998-05-18 | 2008-10-07 | Takeda Pharmaceutical Company Limited | Orally disintegrable tablets |
| US7790755B2 (en) | 2002-10-16 | 2010-09-07 | Takeda Pharmaceutical Company Limited | Controlled release preparation |
| US7815940B2 (en) | 2001-04-18 | 2010-10-19 | Orexo Ab | Gastric acid secretion inhibiting composition |
| WO2011136750A1 (en) * | 2010-04-26 | 2011-11-03 | Mahmut Bilgic | Pharmaceutical compositions inducing synergistic effect |
| US8105626B2 (en) | 2001-10-17 | 2012-01-31 | Takeda Pharmaceutical Company Limited | Granules containing acid-unstable chemical in large amount |
| JP2012031189A (ja) * | 1998-11-05 | 2012-02-16 | Astrazeneca Ab | オメプラゾール含有医薬製剤 |
| WO2011108826A3 (en) * | 2010-03-04 | 2012-03-01 | Hanmi Holdings Co., Ltd. | Complex formulation for oral administration comprising probiotic formulation and 5-ht4 receptor agonist and method for the preparation thereof |
| WO2012162777A1 (pt) * | 2011-06-03 | 2012-12-06 | Eurofarma Laboratórios S.A | Composição farmacêutica oral compreendendo um inibidor de bomba de prótons e um agente procinético para uso em transtornos de excesso de ácido gástrico |
| USRE45198E1 (en) | 1996-01-04 | 2014-10-14 | The Curators Of The University Of Missouri | Omeprazole solution and method for using same |
| US8906940B2 (en) | 2004-05-25 | 2014-12-09 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| US8993599B2 (en) | 2003-07-18 | 2015-03-31 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| US8991390B2 (en) | 2010-01-05 | 2015-03-31 | Microdose Therapeutx, Inc. | Inhalation device and method |
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| US6645988B2 (en) | 1996-01-04 | 2003-11-11 | Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and method of using same |
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| SE510650C2 (sv) | 1997-05-30 | 1999-06-14 | Astra Ab | Ny förening |
| ES2137862B1 (es) * | 1997-07-31 | 2000-09-16 | Intexim S A | Preparacion farmaceutica oral que comprende un compuesto de actividad antiulcerosa y procedimiento para su obtencion. |
| US6521255B2 (en) * | 2000-01-13 | 2003-02-18 | Osmotica Corp. | Osmotic device containing ranitidine and a prokinetic agent |
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| JP2001525366A (ja) * | 1997-12-08 | 2001-12-11 | ビイク グルデン ロンベルク ヒエーミツシエ フアブリーク ゲゼルシヤフト ミツト ベシユレンクテル ハフツング | 酸不安定な活性化合物を含有する新規の投与形 |
| DK173431B1 (da) * | 1998-03-20 | 2000-10-23 | Gea Farmaceutisk Fabrik As | Farmaceutisk formulering omfattende en 2-[[(2-pyridinyl)methyl]sulfinyl]benzimidazol med anti-ulcusaktivitet samt fremgangs |
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