WO1995001977A1 - Magnesium omeprazole - Google Patents

Magnesium omeprazole Download PDF

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Publication number
WO1995001977A1
WO1995001977A1 PCT/SE1994/000680 SE9400680W WO9501977A1 WO 1995001977 A1 WO1995001977 A1 WO 1995001977A1 SE 9400680 W SE9400680 W SE 9400680W WO 9501977 A1 WO9501977 A1 WO 9501977A1
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WO
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Prior art keywords
magnesium omeprazole
magnesium
omeprazole
determined
crystals
Prior art date
Application number
PCT/SE1994/000680
Other languages
French (fr)
Other versions
WO1995001977A9 (en
Inventor
Lars Åke KÄLLSTRÖM
Monica Annelie Nygren
Original Assignee
Astra Aktiebolag
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Priority to DK94921154T priority Critical patent/DK0707580T3/en
Priority to SK22-96A priority patent/SK281230B6/en
Priority to RU96102079A priority patent/RU2139868C1/en
Priority to AT94921154T priority patent/ATE212628T1/en
Priority to DE0707580T priority patent/DE707580T1/en
Priority to JP50400595A priority patent/JP3635432B2/en
Priority to DE69429774T priority patent/DE69429774T2/en
Priority to UA96010059A priority patent/UA43343C2/en
Priority to EP94921154A priority patent/EP0707580B1/en
Application filed by Astra Aktiebolag filed Critical Astra Aktiebolag
Priority to US08/313,342 priority patent/US5900424A/en
Priority to PL94312440A priority patent/PL175999B1/en
Priority to BR9406940A priority patent/BR9406940A/en
Priority to HU9503873A priority patent/HU226861B1/en
Priority to SI9430414T priority patent/SI0707580T1/en
Priority to AU71981/94A priority patent/AU679766B2/en
Publication of WO1995001977A1 publication Critical patent/WO1995001977A1/en
Priority to NO960068A priority patent/NO308702B1/en
Priority to FI960101A priority patent/FI114154B/en
Publication of WO1995001977A9 publication Critical patent/WO1995001977A9/en
Priority to GR970300015T priority patent/GR970300015T1/en
Priority to HK98109227A priority patent/HK1008329A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • 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 relates to a novel process for manufacturing the magnesium salt of omeprazole; the magnesium salt of omeprazole in a novel physical form, especially the magnesium salt as a product of the novel process; the use of the novel form of the magnesium salt of omeprazole in the manufacture of pharmaceutical formulations; and to the use of the novel form of the magnesium salt of omeprazole in medicine.
  • Omeprazole is useful for inhibiting gastric acid secretion and has gastric mucosa protective activity in mammals and man.
  • omeprazole may be used for prevention and treatment of gastric a- .d related disorders and gastrointestinal inflammatory diseases in mammal and man, including e.g. gastritis, gastric ulcer and duodenal ulcer.
  • omeprazole designates the neutral form of the compound, that is the form without a salt forming cation present.
  • magnesium omeprazole salts are very fragile making processes utilising such crystals less attractive in full scale production. Performing the process without crystallization of the magnesium omeprazole gives a product which is less suitable as a pharmaceutical substance.
  • magnesium omeprazole in this specification denoted magnesium omeprazole
  • One object of the present invention is to provide a process for full scale production of magnesium omeprazole.
  • a further object of the present invention is to provide a novel form of the magnesium salt of omeprazole which can be used in full scale manufacturing of pharmaceutical formulations, such as tablets.
  • the combination of physical properties of the novel magnesium omeprazole product of the present invention with respect to the degree of crystallinity, particle diameter, density, hygroscopicity, water content and content of other solvents are favorable and permit the manufacture of magnesium omeprazole in a form which possesses the desired properties.
  • novel form of magnesium omeprazole can also be formulated into other forms for oral administration and other types of administration such as rectal administration.
  • examples of formulations are tablets, pellets, granules, capsules, suspensions and suppositories.
  • the novel process for the manufacture of magnesium omeprazole also circumvents the above described manufacturing problems and renders possible the recovery and work-up of the magnesium omeprazole substance in traditional chemical process equipment.
  • MMD mean mass diameter
  • the invention also relates to a process for manufacturing the novel form of magnesium omeprazole. This process is described in more detail below.
  • the invention relates to all of the aspects given under Field of the invention.
  • a lower alcohol such as methanol, ethanol, n-propanol or iso-propanol, preferably methanol
  • a solution of polar solvents with a weighed amount of magnesium at temperatures between 0°C and reflux temperature.
  • the temperature should preferably be between 10 and 30°C.
  • the temperature can, in a second step be raised further to between 0°C and reflux temperature, preferably 20-50°C.
  • the temperature is reduced to 0-40°C, preferably 10-25°C.
  • Omeprazole or a salt of omeprazole is then added to the solution and after termination of the reaction the mixture is cooled to -10°C to +20°C, preferably -5°C to +5°C.
  • the solvent is then evaporated to 40-60% of the initial volume, which makes the inorganic salts precipitate.
  • the precipitate is separated from the reaction solution for example by centrifugation or filtration and the solution is heated to 5°C to 30°C whereafter the solution is seeded with magnesium omeprazole crystals.
  • An amount of water which is approximately equal to the volume of the solution, is added to start the crystallization.
  • the solution is cooled to -10 to +20°C, preferably 0-10°C to complete the crystallization.
  • the crystals are then separated from the mother liquid for example by centrifugation or filtration and washed with polar solvents preferably an aqueous lower alcohol such as aqueous methanol. Finally, the produced crystals are dried preferably under reduced pressure and heating.
  • the process for manufacturing the new form of magnesium omeprazole differs from the earlier known processes in that the product is recovered after a controlled crystallization step in aqueous alcohol, preferably methanol by, first, separating the inorganic salts from the mother liquour.
  • the crystallinity resulting from this step is, unexpectedly, higher and the product possesses a higher degree of purity and is more stable to decomposition from uptake of moisture.
  • the drying step can be performed without caking.
  • the new process is possible to perform in conventional chemical process equipment and gives a product with a higher yield than the processes hitherto known.
  • Example 1 The following detailed Example 1 will serve to more fully illustrate the process for manufacturing magnesium omeprazole in full scale according to the present invention.
  • sample A is manufactured according to this example.
  • a reactor was filled with 2026 litres of methanol. The stirrer was started and the temperature was adjusted to 20°C. 3,90 kg of magnesium was added to the vessel and immediately thereafter 1,0 litre of Cr ⁇ Ck,. The reactor was heated to 40°C and kept at this temperature for 60 min. It was then cooled to 15°C before the addition of 99,9 kg of omeprazole. The reactor was kept at this temperature for 60 min and then cooled to 0°C. The temperature was kept at this level for 30 minutes before 1000 1 of methanol were evaporated under vacuum and the inorganic solid salt was separated from the liquid first by centrifugation and then by filtration.
  • the liquid was heated to 10°C and the liquid was seeded with magnesium omeprazole crystals whereafter the magnesium omeprazole salt was precipitated by addition of 900 1 of water.
  • the mixture was then cooled to 5°C. After the crystallization had been completed the magnesium omeprazole crystals were centrifuged off and then washed with a mixture of 50 1 of methanol and 150 1 of water.
  • the produced magnesium omeprazole was dried under reduced pressure finally producing 92,5 kg of crystalline product corresponding to a yield of 81,4%.
  • the novel form of the magnesium salt of omeprazole according to Example 1 possesses the following properties:
  • FIG. 1 A comparison between two different samples of the novel form of magnesium omeprazole of the present invention obtained from two laboratory scale experiments by prior art methods and magnesium omeprazole goes forth from diagrams 1 and 2.
  • sample A represents the novel form of the present invention as manufactured in full scale process equipment
  • Sample B represents the product of preparation via synthesis by treatment of omeprazole with Mg(OCHg)2-
  • Sample C represents the product of preparation via treatment of sodium omeprazole with MgC ⁇ .
  • Figure 1 shows in diagram 1 that the particle size measured as mean mass diameter of the product of method A is 19 ⁇ m which is smaller than the corresponding particle size for the products of method B which is 25 ⁇ m and of method C which is greater than 600 ⁇ m.
  • Figure 2 shows in diagram 2 that the degree of crystallinity of the particles of the product of method A is 76% which is higher than the corresponding figure for the product of sample B, which is 0% and also higher than the corresponding figure of sample C, which 67%. '

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Electroplating Methods And Accessories (AREA)
  • Conductive Materials (AREA)
  • Contacts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Fats And Perfumes (AREA)
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Abstract

A novel compound form of magnesium omeprazole useful in the manufacture of pharmaceutical formulations, the use of the product and the process for its production are described.

Description

MAGNESIUM OMEPRAZOLE
Field of the invention
The present invention relates to a novel process for manufacturing the magnesium salt of omeprazole; the magnesium salt of omeprazole in a novel physical form, especially the magnesium salt as a product of the novel process; the use of the novel form of the magnesium salt of omeprazole in the manufacture of pharmaceutical formulations; and to the use of the novel form of the magnesium salt of omeprazole in medicine.
Background of the invention
The compound known under the generic name omeprazole is described i.a. in European patent specification 0005129.
Omeprazole is useful for inhibiting gastric acid secretion and has gastric mucosa protective activity in mammals and man. In a more general sense, omeprazole may be used for prevention and treatment of gastric a- .d related disorders and gastrointestinal inflammatory diseases in mammal and man, including e.g. gastritis, gastric ulcer and duodenal ulcer.
The term "omeprazole" as used in this specification designates the neutral form of the compound, that is the form without a salt forming cation present.
Certain salts of omeprazole are described in European patent specification 0124495. In said patent specification th requirements and importance regarding storage stability of pharmaceutical preparations are emphasized. Salts possessing superior properties with regard i.a. to storage stability are described in the said European patent specification. In EP 0124495; examples 5 and 6 disclose the synthesis of a magnesium salt of omeprazole.
The isolation and purification in full manufacturing scale of the described magnesium omeprazole salts presents one major problem in that magnesium omeprazole salt crystals are very fragile making processes utilising such crystals less attractive in full scale production. Performing the process without crystallization of the magnesium omeprazole gives a product which is less suitable as a pharmaceutical substance.
In order to use the magnesium salt of omeprazole, in this specification denoted magnesium omeprazole, in full manufacturing scale in preparing pharmaceutical formulations primarily for oral administration, such as tablets, it is necessary that said magnesium omeprazole possesses a combination of properties which makes such full scale manufacturing feasible. One object of the present invention is to provide a process for full scale production of magnesium omeprazole. A further object of the present invention is to provide a novel form of the magnesium salt of omeprazole which can be used in full scale manufacturing of pharmaceutical formulations, such as tablets.
The combination of physical properties of the novel magnesium omeprazole product of the present invention with respect to the degree of crystallinity, particle diameter, density, hygroscopicity, water content and content of other solvents are favorable and permit the manufacture of magnesium omeprazole in a form which possesses the desired properties.
The novel form of magnesium omeprazole can also be formulated into other forms for oral administration and other types of administration such as rectal administration. Examples of formulations are tablets, pellets, granules, capsules, suspensions and suppositories. The invention
We now provide a novel form of the magnesium salt of omeprazole exhibiting the desired combination of physical properties. This makes full scale production of magnesium omeprazole as well as full scale production of pharmaceutical formulations thereof feasible.
The novel process for the manufacture of magnesium omeprazole also circumvents the above described manufacturing problems and renders possible the recovery and work-up of the magnesium omeprazole substance in traditional chemical process equipment.
It has been found that the following property is significant to obtain such product:
a) Crystalline form, with a degree of crystallinity of not less than 70%, preferably higher than 75% as determined by X-ray powder diffraction
It is desirable that the product also exhibits the following properties;
b) Particle size measured as mean mass diameter (MMD) less than 30μm, preferably less than 20 μm as determined by laser diffraction technique.
c) Density between 1.33 g/cm and 1.35 g/cirr 3 as determined by powder pycnometer.
d) Hygroscopicity not exceeding 2% increase of weight upon storage for one month up to 94% relative atmospheric humidity as determined gravimetrically.
e) A content of water of between 5% and 10% by weight as determined by titration according to Karl Fischer. f) A content of methanol less than 0.1% preferably less than 0.05% by weight as determined by gas chromatography, in case methanol is used as solvent.
In a further aspect, the invention also relates to a process for manufacturing the novel form of magnesium omeprazole. This process is described in more detail below.
The invention relates to all of the aspects given under Field of the invention.
The process for producing the novel form of magnesium omeprazole is characterized by the following consecutive steps
a) treating omeprazole or a salt thereof with magnesium alcoholate in a solution
b) separating inorganic salts from the reaction mixture
c) crystallizing magnesium omeprazole
d) isolating the obtained crystalline magnesium omeprazole and, optionally,
e) purifying and drying the crystalline magnesium omeprazole using conventional methods.
The process for manufacturing the new product can be described in the following way.
A lower alcohol, such as methanol, ethanol, n-propanol or iso-propanol, preferably methanol, is treated in a solution of polar solvents with a weighed amount of magnesium at temperatures between 0°C and reflux temperature. The temperature should preferably be between 10 and 30°C. After addition of the magnesium to the solution the temperature can, in a second step be raised further to between 0°C and reflux temperature, preferably 20-50°C. After termination of the reaction the temperature is reduced to 0-40°C, preferably 10-25°C. Omeprazole or a salt of omeprazole is then added to the solution and after termination of the reaction the mixture is cooled to -10°C to +20°C, preferably -5°C to +5°C. The solvent is then evaporated to 40-60% of the initial volume, which makes the inorganic salts precipitate. The precipitate is separated from the reaction solution for example by centrifugation or filtration and the solution is heated to 5°C to 30°C whereafter the solution is seeded with magnesium omeprazole crystals. An amount of water, which is approximately equal to the volume of the solution, is added to start the crystallization. The solution is cooled to -10 to +20°C, preferably 0-10°C to complete the crystallization. The crystals are then separated from the mother liquid for example by centrifugation or filtration and washed with polar solvents preferably an aqueous lower alcohol such as aqueous methanol. Finally, the produced crystals are dried preferably under reduced pressure and heating.
The process for manufacturing the new form of magnesium omeprazole differs from the earlier known processes in that the product is recovered after a controlled crystallization step in aqueous alcohol, preferably methanol by, first, separating the inorganic salts from the mother liquour. The crystallinity resulting from this step is, unexpectedly, higher and the product possesses a higher degree of purity and is more stable to decomposition from uptake of moisture. The drying step can be performed without caking. The new process is possible to perform in conventional chemical process equipment and gives a product with a higher yield than the processes hitherto known.
The following detailed Example 1 will serve to more fully illustrate the process for manufacturing magnesium omeprazole in full scale according to the present invention. In Figures 1 and 2 sample A is manufactured according to this example. Example 1
A reactor was filled with 2026 litres of methanol. The stirrer was started and the temperature was adjusted to 20°C. 3,90 kg of magnesium was added to the vessel and immediately thereafter 1,0 litre of Cr^Ck,. The reactor was heated to 40°C and kept at this temperature for 60 min. It was then cooled to 15°C before the addition of 99,9 kg of omeprazole. The reactor was kept at this temperature for 60 min and then cooled to 0°C. The temperature was kept at this level for 30 minutes before 1000 1 of methanol were evaporated under vacuum and the inorganic solid salt was separated from the liquid first by centrifugation and then by filtration. The liquid was heated to 10°C and the liquid was seeded with magnesium omeprazole crystals whereafter the magnesium omeprazole salt was precipitated by addition of 900 1 of water. The mixture was then cooled to 5°C. After the crystallization had been completed the magnesium omeprazole crystals were centrifuged off and then washed with a mixture of 50 1 of methanol and 150 1 of water. The produced magnesium omeprazole was dried under reduced pressure finally producing 92,5 kg of crystalline product corresponding to a yield of 81,4%.
The novel form of the magnesium salt of omeprazole according to Example 1 possesses the following properties:
a) Crystalline form, with a degree of crystallinity of 76%, as determined by X-ray powder diffraction.
b) Particle size measured as mean mass diameter (MMD) of 19μm as determined by laser diffraction technique.
c) Density of 1.342 g/cm as determined by powder pycnometer.
d) Hygroscopicity of 1.62% increase of weight upon storage for one month at 94% relative atmospheric humidity as determined gravimetrically. e) Content of moisture water of 7.6 by weight as determined by titration according to Karl Fischer.
f) Content of methanol of 0.006% by weight as determined by gas chromatography.
A comparison between two different samples of the novel form of magnesium omeprazole of the present invention obtained from two laboratory scale experiments by prior art methods and magnesium omeprazole goes forth from diagrams 1 and 2. In these diagrams sample A represents the novel form of the present invention as manufactured in full scale process equipment Sample B represents the product of preparation via synthesis by treatment of omeprazole with Mg(OCHg)2- Sample C represents the product of preparation via treatment of sodium omeprazole with MgC^.
Figure 1 shows in diagram 1 that the particle size measured as mean mass diameter of the product of method A is 19 μm which is smaller than the corresponding particle size for the products of method B which is 25 μm and of method C which is greater than 600 μm.
Figure 2 shows in diagram 2 that the degree of crystallinity of the particles of the product of method A is 76% which is higher than the corresponding figure for the product of sample B, which is 0% and also higher than the corresponding figure of sample C, which 67%. '

Claims

1. Magnesium omeprazole characterized in having a degree of crystallinity which is higher than 70% as determined by X-ray powder diffraction.
2. Magnesium omeprazole according to claim 1 wherein the degree of crystallinity is higher than 75%.
3. Magnesium omeprazole according to claim 1 wherein the mean particle diameter as determined by laser diffraction technique is less than 30μm, and preferably less than 20μm.
4. Magnesium omeprazole according to claim 1 wherein the density is between
1.33 g/cm and 1.35 g/cm 3 as determined by powder pycnometer.
5. Magnesium omeprazole according to claim 1 wherein the hygroscopicity is less than 2% increase of weight upon storage for one month at up to 94% relative atmospheric humidity as determined by gravimetry.
6. Magnesium omeprazole according to claim 1 wherein the water content is between 5% and 10% by weight as determined by titration according to Karl Fischer.
7. Magnesium omeprazole according to claim 1 containing less than 0.1 % by weight of solvent as determined by gas chromatography.
8. Magnesium omeprazole according to claim 1 containing less than 0.05% by weight of solvent as determined by gas chromatography.
9. A process for the manufacture of magnesium omeprazole according to any of claims 1 to 8 characterized by in consecutive steps a) treating omeprazole or a salt thereof with magnesium alcoholate in a solution,
b) separating inorganic salts from the reaction mixture,
c) crystallizing magnesium omeprazole,
d) isolating the obtained crystalline magnesium omeprazole and, optionally,
e) purifying and drying the crystalline magnesium omeprazole using conventional methods.
10. A process according to Claim 9 wherein the magnesium alcoholate is magnesium methyl alcoholate.
11. A process according to claim 9 wherein the solvent is methanol.
12. A process according to claim 9 wherein the crystallization is accomplished by addition of water.
13. A process according to claim 9 wherein the isolation of the magnesium omeprazole is performed by centrifugal separation of the crystals.
14. A process according to claim 9 wherein the isolation of the magnesium omeprazole is performed by crystallization followed by filtration of the crystals.
15. A process according to claim 9 wherein the purification of the magnesium omeprazole crystals is performed by washing the crystals with a solution of polar solvents.
16. A process according to claim 9 wherein the magnesium omeprazole crystals are dried preferably under reduced pressure.
17. A process according to claim 9 wherein the drying of the magnesium omeprazole crystals is performed by evaporating the remaining solvent by heating.
18. Magnesium omeprazole obtained by a process according to any of claims 9 to 17.
19. A pharmaceutical composition containing magnesium omeprazole according to any of claims 1 to 8 as an active ingredient.
20. A pharmaceutical formulation for oral administration containing magnesium omeprazole according to any of claims 1 to 8 as an active ingredient.
21. A tablet formulation containing magnesium omeprazole according to any of claims 1 to 8 as an active ingredient.
22. Magnesium omeprazole according to any of claims 1 to 8 for use in therapy.
23. Magnesium omeprazole according to any of claims 1 to 8 for use in inhibiting gastric acid secretion in mammals and man.
24. Magnesium omeprazole according to any of claims 1 to 8 for use as an agent with gastric mucosa protective activity in mammals and man.
25. Magnesium omeprazole according to any of claims 1 to 8 for use in the treatment of gastric acid related diseases in mammals and man.
26. The use of magnesium omeprazole according to any of claims 1 to 8 in the manufacture of a medicament for inhibiting gastric acid secretion.
27. The use of magnesium omeprazole according to any of claims 1 to 8 in the manufacture of a medicament for obtaining gastric mucosa protective activity.
28. The use of magnesium omeprazole according to any of claims 1 to 8 in the manufacture of a medicament for the treatment of gastric acid related diseases.
29. A method for inhibiting gastric acid secretion in mammals and man by administering to a host in need thereof a therapeutically effective dose of magnesium omeprazole according to any of claims 1 to 8.
30. A method for the treatment of gastric acid related diseases in mammals and man by administering to a host in need thereof a therapeutically effective dose of magnesium omeprazole according to any of claims 1 to 8.
PCT/SE1994/000680 1993-07-09 1994-07-08 Magnesium omeprazole WO1995001977A1 (en)

Priority Applications (19)

Application Number Priority Date Filing Date Title
US08/313,342 US5900424A (en) 1993-07-09 1994-07-08 Omeprazole magnesium salt form
PL94312440A PL175999B1 (en) 1993-07-09 1994-07-08 Magnezium omeprazol
SK22-96A SK281230B6 (en) 1993-07-09 1994-07-08 Omeprazole magnesium, process for its manufacture, pharmaceuticals it containing, and use of omeprazole magnesium
AT94921154T ATE212628T1 (en) 1993-07-09 1994-07-08 MAGNESIUM OMEPRAZOLE
DE0707580T DE707580T1 (en) 1993-07-09 1994-07-08 MAGNESIUM OMEPRAZOL
JP50400595A JP3635432B2 (en) 1993-07-09 1994-07-08 Manufacturing method of omeprazole magnesium
DE69429774T DE69429774T2 (en) 1993-07-09 1994-07-08 MAGNESIUM OMEPRAZOL
UA96010059A UA43343C2 (en) 1993-07-09 1994-07-08 Magnesium omeprazole, process for preparation thereof, pharmaceutical composition, treatment method
BR9406940A BR9406940A (en) 1993-07-09 1994-07-08 Magnesium-omeprazole process for the preparation of magnesium-omeprazole pharmaceutical composition pharmaceutical formulation for oral administration forum use of magnesium-omeprazole process for the inhibition of gastric acid secretion in mammals and in man and process for the treatment of diseases related to gastric acid in mammals and in men
DK94921154T DK0707580T3 (en) 1993-07-09 1994-07-08 Magnesium
AU71981/94A AU679766B2 (en) 1993-07-09 1994-07-08 Magnesium omeprazole
RU96102079A RU2139868C1 (en) 1993-07-09 1994-07-08 Omeprazole magnesium salt, method of its preparing, pharmaceutical composition, method of treatment
EP94921154A EP0707580B1 (en) 1993-07-09 1994-07-08 Magnesium omeprazole
HU9503873A HU226861B1 (en) 1993-07-09 1994-07-08 Magnesium salt of omeprazole
SI9430414T SI0707580T1 (en) 1993-07-09 1994-07-08 Magnesium omeprazole
NO960068A NO308702B1 (en) 1993-07-09 1996-01-05 Magnesium omeprazole, process for its preparation, pharmaceutical composition containing magnesium omeprazole and use thereof
FI960101A FI114154B (en) 1993-07-09 1996-01-09 A process for the preparation of a therapeutically useful magnesium omeprazole
GR970300015T GR970300015T1 (en) 1993-07-09 1997-05-30 Magnesium omeprazole
HK98109227A HK1008329A1 (en) 1993-07-09 1998-07-17 Magnesium omeprazole

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE19939302396A SE9302396D0 (en) 1993-07-09 1993-07-09 A NOVEL COMPOUND FORM
SE9302396-8 1993-07-09

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WO1995001977A1 true WO1995001977A1 (en) 1995-01-19
WO1995001977A9 WO1995001977A9 (en) 1996-02-01

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PCT/SE1994/000680 WO1995001977A1 (en) 1993-07-09 1994-07-08 Magnesium omeprazole

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US (1) US5900424A (en)
EP (2) EP0707580B1 (en)
JP (2) JP3635432B2 (en)
KR (1) KR100353783B1 (en)
CN (1) CN1064680C (en)
AT (1) ATE212628T1 (en)
AU (1) AU679766B2 (en)
BR (1) BR9406940A (en)
CA (1) CA2166794C (en)
CZ (1) CZ288933B6 (en)
DE (2) DE707580T1 (en)
DK (1) DK0707580T3 (en)
DZ (1) DZ1792A1 (en)
EE (1) EE03127B1 (en)
EG (1) EG21437A (en)
ES (1) ES2100136T3 (en)
FI (1) FI114154B (en)
GR (1) GR970300015T1 (en)
HK (1) HK1008329A1 (en)
HR (1) HRP940385B1 (en)
HU (1) HU226861B1 (en)
IL (1) IL110190A (en)
IS (1) IS2075B (en)
MA (1) MA23257A1 (en)
MX (1) MX9405217A (en)
MY (1) MY113274A (en)
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SA94150058B1 (en) 2006-06-20
DK0707580T3 (en) 2002-04-15
HUT75314A (en) 1997-05-28
SK2296A3 (en) 1996-10-02
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CA2166794C (en) 1997-03-04
CN1064680C (en) 2001-04-18
HU9503873D0 (en) 1996-02-28
EP1164132A2 (en) 2001-12-19
PT707580E (en) 2002-06-28
GR970300015T1 (en) 1997-05-31
DE707580T1 (en) 1997-09-04
DZ1792A1 (en) 2002-02-17
ZA944933B (en) 1995-02-20

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