WO2003066045A1 - Kombinationspräparat des natrium-wasserstoff-austauch-inhibitors cariporide mit ace-hemmern zur verhinderung der herzinsuffizienz und anderer altersbedingter organ-dysfunktionen, altersbedingter erkrankungen und zur lebensverlängerung - Google Patents
Kombinationspräparat des natrium-wasserstoff-austauch-inhibitors cariporide mit ace-hemmern zur verhinderung der herzinsuffizienz und anderer altersbedingter organ-dysfunktionen, altersbedingter erkrankungen und zur lebensverlängerung Download PDFInfo
- Publication number
- WO2003066045A1 WO2003066045A1 PCT/EP2003/000587 EP0300587W WO03066045A1 WO 2003066045 A1 WO2003066045 A1 WO 2003066045A1 EP 0300587 W EP0300587 W EP 0300587W WO 03066045 A1 WO03066045 A1 WO 03066045A1
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- WO
- WIPO (PCT)
- Prior art keywords
- age
- cariporide
- ramipril
- combination
- human
- Prior art date
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Classifications
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- 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
- A61K31/13—Amines
- A61K31/155—Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
Definitions
- the invention describes a combination of Cariporide (HOE 642), an inhibitor of the cellular sodium-hydrogen exchanger, with the ACE inhibitor Ramipril, and its application in human and veterinary medicine for the prevention of heart failure and other age-related disorders and dysfunctional changes of Organs of the body and for the prevention of age-related illnesses and for the life extension under currency of an improved quality of life.
- HOE 642 Cariporide
- Ramipril an inhibitor of the cellular sodium-hydrogen exchanger
- WO 00/38661 describes the use of inhibitors of the sodium hydrogen exchange (NHE) in the manufacture of a medicament for the prevention of age-related organ dysfunction, age-related diseases and life extension.
- Inhibitors of the cellular sodium hydrogen exchange agent are described for the manufacture of a medicament for the prevention of age-related dysfunction and dysfunctional changes of organs of the body and for the prevention of age-related diseases and for the prolongation of life while maintaining an improved quality of life.
- NHE sodium hydrogen exchange
- Cariporide and its pharmaceutically acceptable salts are named, for example, the cariporide mesilate having the following formula:
- WO 00/38 661 the biological findings were collected on normotensive healthy rats. Unlike NHE inhibitors, inhibitors of angiotensin converting enzyme (ACE) on the example of ramipril have no protective effect on the described pathological age-related organ changes in old normotensive rats. Furthermore, in WO 00/38661 the combination of NHE inhibitors with antihypertensive drugs, such as ACE inhibitors, angiotensin receptor antagonists, etc., is contemplated to provide, in addition to the old ngsprotektiven effect of NHE inhibitors the potential benefit of a blood pressure lowering effect of hypotensives to use. An increase in a life-prolonging effect or a protective effect on pathological age-related organ changes was not expected.
- ACE angiotensin converting enzyme
- NHE inhibitors alone and in combination with ACE inhibitors also on spontaneous hypertensive rats (SHR) cause a significant life-prolonging effect and a protective effect on pathological age-related organ changes.
- SHR spontaneous hypertensive rats
- ramipril was used in subliminal dose with regard to lowering blood pressure.
- non-hypotensive action resulted in significantly more favorable alterative-selective effects.
- the combination treatment is significantly superior to both single preparations.
- a subliminal, non-hypotensive dose of ramipril is usually in the range of 1 to 50 ⁇ g per kg of body weight per day in the rat.
- a subliminal dose of ramipril when administered to a subject of about 70 kg body weight is generally in a range of 0.1 to 1.0 mg per day and human, preferably 0.3 to 0.7 mg per day and human, for example at 0.625 mg per day and human.
- the model of these hypertensive rats is generally considered to be representative of human essential hypertension.
- 27 hypertensive rats were used at the age of 18 months.
- the hearts of low-dose ramipril-treated SHRs showed a significant reduction in cardiac output compared to placebo control hearts.
- cariporide and the ramipril / cariporide combination significantly improved cardiac function.
- the myocardial fibrosis correlating with heart failure was significantly reduced by cariporide monotherapy as well as by the ramipril / cariporide combination.
- the significantly lower heart weights also show the antifibrotic effect of the Ramipril / Cariporide combination and cariporide directed against the development of heart failure.
- the single preparations ramipril and cariporide lead to an improvement in survival compared to placebo treatment. Significant differences in the survival rates of cariporide and ramipril could not be detected.
- the cariporide-ramipril combination leads to a significant increase in the survival rate in comparison with the effects produced by the individual compounds.
- Cariporide can thus be used according to the invention together with ramipril on the animal, preferably on the mammal, and in particular on humans in an advantageous manner as a medicament.
- the invention relates to the combination of cariporide and ramipril for use in human medicine and veterinary medicine, for example in dogs.
- the combination of the two drugs may be such that cariporide and ramipril are co-administered in a drug (combination preparation) or that a drug containing a cariporide drug and a separate drug containing ramipril are administered simultaneously or sequentially in any order.
- Administration in sequence also includes a combination in which the individual drugs are administered at different times and in different ways to achieve a better effect.
- the cariporide and the ramipril in the form of a pharmaceutical combination preparation in which the two active ingredients are present in a fixed ratio, or to administer them in the form of separate pharmaceutical single preparations.
- the individual preparations may be in a suitable primary packaging and optionally together with a reference to the inventive use instructions in a common packaging, or the individual preparations may optionally together with on the "inventive use referencing instructions in separate packages are located. All such products and preparation species are encompassed by the present invention.
- Combinations are usually in a range from 1: 0.0001 to 1: 1, preferably between 1: 0.0001 and 1: 0.1, for example between 1: 0.0005 and 1: 0.01.
- the present invention relates to pharmaceutical preparations containing as active ingredient both Cariporide and Ramipril in addition to conventional; contain pharmaceutically acceptable carriers and excipients.
- the pharmaceutical preparations normally contain 0.01 to 90% by weight cariporide and ramipril.
- the preparation of the pharmaceutical preparations can be carried out in a manner known per se.
- the active ingredients are brought together with one or more solid or liquid galenic excipients and / or excipients in a suitable dosage form or dosage form, which can then be used as a medicament in human medicine or veterinary medicine.
- pharmaceutical preparations used according to the invention which contain the active ingredients Cariporide and Ramipril separately.
- the present invention also provides the use of cariporide and ramipril for the preparation of a pharmaceutical preparation and their use as a medicament for inhibiting the development of age-related diseases in human or veterinary medicine, for inhibiting the development of age-related Organ damage, to extend life and / or to prevent or inhibit the further progression of heart failure or partial regression of the disease.
- the dosage of the active substances cariporide and / or ramipril to be administered depends on the individual case and, as usual, must be adapted to the circumstances of the individual case for optimum effect. Of course, it depends on the frequency of administration and on the type of galenic formulations used in each case for therapy or prophylaxis, but also on the type and strength of the disease to be treated and on sex, age, weight and individual responsiveness of the person or animal to be treated and whether it is acute or chronic therapy or prophylaxis.
- the dosage of ramipril may vary in the range of 0.1 to 10 mg per day and per human (at about 70 kg of body weight), preferably from 0.1 to 5 mg per day and human, more preferably from 0.2 to 2.5 mg per day and human.
- the ramipril dose may also be given in a subliminal range of 0.1 to 1 mg per day and human, preferably from 0.3 to 0.7 mg per day and human.
- the dose may vary between 50 mg and 1 g per day and human, preferably between 100 to 500 mg per day and human.
- the ramipril dose may be 0.625 mg per day and human and the cariporide dose 200 mg per day and human.
- Cariporide and Ramipril can be administered in lower doses than when only one of the two active substances is administered.
- the daily dose of the active ingredients may be administered at one time or may be divided into several, for example two, three or four, administrations.
- Medicaments containing combinations of cariporide and ramipril according to the invention may be administered orally, parenterally, e.g. B are administered intravenously, rectally, transdermally or topically, the preferred application depending on the individual case.
- excipients are suitable for the desired drug formulation is familiar to the person skilled in the art on the basis of his specialist knowledge.
- solvents for example, antioxidants, dispersants, emulsifiers, defoamers, flavoring agents, preservatives, solubilizers, means for obtaining a depot effect, buffer substances or dyes.
- the active compounds with the appropriate additives such as carriers, stabilizers or inert diluents, mixed and brought by the usual methods in the appropriate dosage forms, such as tablets, dragees, capsules, aqueous, alcoholic or oily solutions.
- inert carrier can z. Gum arabic, magnesia, magnesium carbonate, potassium phosphate, lactose, glucose or starch, especially corn starch.
- the preparation can be carried out both as a dry and as a wet granules.
- Suitable oily carriers or as solvents are, for example, vegetable or animal oils, such as sunflower oil or cod liver oil.
- solvents for aqueous or alcoholic solutions come z.
- Other auxiliaries also for other forms of application, are for.
- the active compounds for subcutaneous or intravenous administration, the active compounds, if desired with the customary substances such as solubilizers, emulsifiers or other auxiliaries, in solution, suspension or emulsion.
- a solvent come z.
- physiological saline or alcohols eg. As ethanol, propanol, glycerol, into consideration, besides also
- 27 hypertensive rats at the age of 18 months were used.
- 400 mg / kg body weight of cariporide was administered via the diet (0.6% cariporide in standard rat diet) and 10 ⁇ g / kg body weight of ramipril through the drinking water.
- Fig. 1 shows the progress of the survival rate for all treatment groups in detail. Significant differences between placebo and preparation groups on the one hand, and between the individual preparations and the combination are already evident after a test period of 3 - 4 months.
- Table 3 shows the results of all pairwise comparisons of two treatment groups. The test results are at a multiple significance level of 5%.
- Table 4 shows estimates of median downtime, the time at which the survival rate in the experimental animal population reaches just 50%.
- the proportion of surviving animals in the placebo group has already fallen to 50% after 1.5 months, whereas this is only expected after 8 months for a combined treatment.
- the individual preparations achieve a median survival of 4 months less than half of the combined preparation.
- the individual drugs ramipril and cariporide lead to a statistically significant improvement in survival compared to placebo treatment.
- the old spontaneously hypertensive animals undergo processes of transformation in the myocardial tissue that essentially correspond to those that occur in humans (in the early phase (10th to 15th month of life) compensated heart failure with hypertrophy (NYHA stage 1) -ll), in the later phase (16th - 21st month of life) decompensated heart failure with ventricular dilatation and fibrosis (NYHA stage III-IV)).
- Fig.1 Kaplan-Meier survival times
- FIG. 2 Influence of late treatment with cariporide and ramipril on the myocardial fibrosis of old spontaneously hypertensive rats
- Y axis preparation groups
- Hyp / Arg is the ratio of hydroxyproline to arginine and is considered to be a marker for fibrosing
- FIG. 3 Influence of a late treatment with cariporide and ramipril on the heart weight of spontaneously hypertensive rats
- Y axis preparation groups
- X axis mg heart weight per 100 g body weight Q total heart ⁇ Left ventricle Right ventricle
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- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cardiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hospice & Palliative Care (AREA)
- Heart & Thoracic Surgery (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
Description
Claims
Priority Applications (13)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2003244430A AU2003244430A1 (en) | 2002-02-04 | 2003-01-22 | Combination preparation of the sodium-hydrogen exchange inhibitor cariporide with ace inhibitors for preventing heart failure and other age-related dysfunctions of organs, age- related diseases and for prolonging lifespan |
KR10-2004-7012005A KR20040083498A (ko) | 2002-02-04 | 2003-01-22 | 심부전증 및 기타 노화-관련된 기관의 기능장애,노화-관련 질환을 예방하고 생명을 연장하기 위한 ace억제제와 나트륨-수소 교환 억제제 카리포리드와의 배합제제 |
YUP-682/04A RS68204A (en) | 2002-02-04 | 2003-01-22 | Combination preparation of the sodium- hydrogen exchange inhibitor cariporide with ace inhibitors for preventing heart failure and other age-related dysfunctions of organs, age-related diseases and for prolonging lifespan |
AT03737262T ATE520398T1 (de) | 2002-02-04 | 2003-01-22 | Kombinationspräparat des natrium-wasserstoff- austausch-inhibitors cariporide mit ramipril zur verhinderung bzw zur hemmung der herzinsuffizienz |
EP03737262A EP1474134B1 (de) | 2002-02-04 | 2003-01-22 | Kombinationspräparat des natrium-wasserstoff-austausch-inhibitors cariporide mit ramipril zur verhinderung bzw zur hemmung der herzinsuffizienz |
CA002474888A CA2474888A1 (en) | 2002-02-04 | 2003-01-22 | Combination preparation of the sodium-hydrogen exchange inhibitor cariporide with ace inhibitors for preventing heart failure and other age-related dysfunctions of organs, age-related diseases and for prolonging lifespan |
JP2003565469A JP4733348B2 (ja) | 2002-02-04 | 2003-01-22 | 心不全、他の加齢関連臓器機能不全および加齢関連障害の予防のための、ならびに寿命を延長するための、ナトリウム−水素交換阻害剤であるカリポライドとace阻害剤との組み合わせ製剤 |
NZ534479A NZ534479A (en) | 2002-02-04 | 2003-01-22 | Combination preparation of the sodium-hydrogen exchange inhibitor cariporide with ACE inhibitors for preventing heart failure and other age-related dysfunctions of organs, age-related diseases and for prolonging lifespan |
BR0307443-9A BR0307443A (pt) | 2002-02-04 | 2003-01-22 | Preparado de combinação do inibidor da troca sódio-hidrogênio cariporide com inibidores ace para o impedimento da insuficiência cardìaca e de outras disfunções de órgão condicionadas pela idade, doenças condicionadas pela idade e para o prolongamento da vida |
HU0402593A HUP0402593A2 (hu) | 2002-02-04 | 2003-01-22 | Kariporidból és ramiprilből álló kombinációs készítmény és alkalmazása |
MXPA04007569A MXPA04007569A (es) | 2002-02-04 | 2003-01-22 | Preparacion de la combinacion del inhibidor del intercambio sodio-hidrogeno cariporida con inhibidores ace para evitar la insuficiencia cardiaca y otras disfunciones de los organos relacionadas con la edad, padecimientos relacionados con la edad y pa |
HR20040702A HRP20040702A2 (en) | 2002-02-04 | 2004-08-03 | Combination preparation of the sodium-hydrogen exchange inhibitor cariporide with ace inhibitors forpreventing heart failure and other age-related dysfunctions of organs, age-related diseases and forprolonging lifespan |
NO20043698A NO20043698L (no) | 2002-02-04 | 2004-08-31 | Kombinasjonspreparat av natrium-hydrogenbytteinhibitoren cariporid med ACE-inhibitorer for prevensjon av hjertesvikt og andre aldersrelaterte dysfunksjoner i organer, aldersrelaterte sykdommer og for forlenget levetid |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10204571.2 | 2002-02-04 | ||
DE10204571 | 2002-02-04 |
Publications (1)
Publication Number | Publication Date |
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WO2003066045A1 true WO2003066045A1 (de) | 2003-08-14 |
Family
ID=27674558
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2003/000587 WO2003066045A1 (de) | 2002-02-04 | 2003-01-22 | Kombinationspräparat des natrium-wasserstoff-austauch-inhibitors cariporide mit ace-hemmern zur verhinderung der herzinsuffizienz und anderer altersbedingter organ-dysfunktionen, altersbedingter erkrankungen und zur lebensverlängerung |
Country Status (23)
Country | Link |
---|---|
EP (1) | EP1474134B1 (de) |
JP (1) | JP4733348B2 (de) |
KR (1) | KR20040083498A (de) |
CN (1) | CN1319528C (de) |
AR (1) | AR038387A1 (de) |
AT (1) | ATE520398T1 (de) |
AU (1) | AU2003244430A1 (de) |
BR (1) | BR0307443A (de) |
CA (1) | CA2474888A1 (de) |
CO (1) | CO5601009A2 (de) |
HR (1) | HRP20040702A2 (de) |
HU (1) | HUP0402593A2 (de) |
MA (1) | MA27170A1 (de) |
MX (1) | MXPA04007569A (de) |
NO (1) | NO20043698L (de) |
NZ (1) | NZ534479A (de) |
PE (1) | PE20040188A1 (de) |
PL (1) | PL370488A1 (de) |
RS (1) | RS68204A (de) |
RU (1) | RU2004126702A (de) |
TW (1) | TW200306850A (de) |
WO (1) | WO2003066045A1 (de) |
ZA (1) | ZA200406066B (de) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2795053A1 (en) * | 2010-03-31 | 2011-10-06 | The Hospital For Sick Children | Use of remote ischemic conditioning to improve outcome after myocardial infarction |
Citations (4)
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DE19734693A1 (de) * | 1997-08-11 | 1998-01-22 | Hoechst Marion Roussel De Gmbh | Verwendung von Cariporide als Inhibitor des zellulären NA+/H+-Exchangers (NHE) zur Herstellung eines Medikaments zur Behandlung von cardialen und nichtcardialen Krankheiten |
EP0855392A2 (de) * | 1997-01-22 | 1998-07-29 | Hoechst Aktiengesellschaft | Fünfgliedrige Heterocyclen mit Biphenylsulfonylsubstitution, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
EP0937464A2 (de) * | 1997-08-27 | 1999-08-25 | Hoechst Marion Roussel Deutschland GmbH | Pharmazeutisches Kombinationspräparat aus eiem Inhibitor des Natrium-Wasserstoff-Austauschers und einem Arzneimittel zur Behandlung von Herz-Kreislauferkrankungen |
DE19859727A1 (de) * | 1998-12-23 | 2000-06-29 | Aventis Pharma Gmbh | Die Verwendung von Hemmern des Natrium-Wasserstoff-Austauschers zur Herstellung eines Medikaments zur Verhinderung von altersbedingten Organ-Dysfunktionen, altersbedingten Erkrankungen zur Lebensverlängerung |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6011059A (en) * | 1997-12-24 | 2000-01-04 | Bristol-Myers Squibb Company | Acyl guanidine sodium/proton exchange inhibitors and method |
-
2003
- 2003-01-22 KR KR10-2004-7012005A patent/KR20040083498A/ko not_active Application Discontinuation
- 2003-01-22 AU AU2003244430A patent/AU2003244430A1/en not_active Abandoned
- 2003-01-22 BR BR0307443-9A patent/BR0307443A/pt not_active IP Right Cessation
- 2003-01-22 RU RU2004126702/15A patent/RU2004126702A/ru not_active Application Discontinuation
- 2003-01-22 PL PL03370488A patent/PL370488A1/xx not_active Application Discontinuation
- 2003-01-22 NZ NZ534479A patent/NZ534479A/xx unknown
- 2003-01-22 RS YUP-682/04A patent/RS68204A/sr unknown
- 2003-01-22 WO PCT/EP2003/000587 patent/WO2003066045A1/de active Application Filing
- 2003-01-22 EP EP03737262A patent/EP1474134B1/de not_active Expired - Lifetime
- 2003-01-22 CN CNB03803185XA patent/CN1319528C/zh not_active Expired - Fee Related
- 2003-01-22 HU HU0402593A patent/HUP0402593A2/hu unknown
- 2003-01-22 AT AT03737262T patent/ATE520398T1/de active
- 2003-01-22 CA CA002474888A patent/CA2474888A1/en not_active Abandoned
- 2003-01-22 MX MXPA04007569A patent/MXPA04007569A/es not_active Application Discontinuation
- 2003-01-22 JP JP2003565469A patent/JP4733348B2/ja not_active Expired - Fee Related
- 2003-01-29 TW TW092101906A patent/TW200306850A/zh unknown
- 2003-01-31 PE PE2003000115A patent/PE20040188A1/es not_active Application Discontinuation
- 2003-01-31 AR ARP030100296A patent/AR038387A1/es unknown
-
2004
- 2004-07-27 MA MA27801A patent/MA27170A1/fr unknown
- 2004-07-29 ZA ZA200406066A patent/ZA200406066B/en unknown
- 2004-08-03 HR HR20040702A patent/HRP20040702A2/hr not_active Application Discontinuation
- 2004-08-03 CO CO04075091A patent/CO5601009A2/es not_active Application Discontinuation
- 2004-08-31 NO NO20043698A patent/NO20043698L/no not_active Application Discontinuation
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EP0855392A2 (de) * | 1997-01-22 | 1998-07-29 | Hoechst Aktiengesellschaft | Fünfgliedrige Heterocyclen mit Biphenylsulfonylsubstitution, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
DE19734693A1 (de) * | 1997-08-11 | 1998-01-22 | Hoechst Marion Roussel De Gmbh | Verwendung von Cariporide als Inhibitor des zellulären NA+/H+-Exchangers (NHE) zur Herstellung eines Medikaments zur Behandlung von cardialen und nichtcardialen Krankheiten |
EP0937464A2 (de) * | 1997-08-27 | 1999-08-25 | Hoechst Marion Roussel Deutschland GmbH | Pharmazeutisches Kombinationspräparat aus eiem Inhibitor des Natrium-Wasserstoff-Austauschers und einem Arzneimittel zur Behandlung von Herz-Kreislauferkrankungen |
DE19859727A1 (de) * | 1998-12-23 | 2000-06-29 | Aventis Pharma Gmbh | Die Verwendung von Hemmern des Natrium-Wasserstoff-Austauschers zur Herstellung eines Medikaments zur Verhinderung von altersbedingten Organ-Dysfunktionen, altersbedingten Erkrankungen zur Lebensverlängerung |
Non-Patent Citations (2)
Title |
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LINZ WOLFGANG ET AL: "Long-term ACE inhibition doubles lifespan of hypertensive rats.", CIRCULATION, vol. 96, no. 9, 4 November 1997 (1997-11-04), pages 3164 - 3172, XP002239742, ISSN: 0009-7322, Retrieved from the Internet <URL:http://circ.ahajournals.org/cgi/content/full/96/9/3164> [retrieved on 20030428] * |
RUETTEN HARTMUT ET AL: "The NHE1 inhibitor cariporide improves left ventricular morphology and function in rats with chronic heart failure in combination with the ACE inhibitor ramipril.", CIRCULATION, vol. 106, no. 19 Supplement, 5 November 2002 (2002-11-05), Abstracts from Scientific Sessions;Chicago, IL, USA; November 17-20, 2002, pages II - 292, XP001147832, ISSN: 0009-7322, Retrieved from the Internet <URL:http://aha.agora.com/abstractviewer/av_view.asp> [retrieved on 20030429] * |
Also Published As
Publication number | Publication date |
---|---|
JP2005519072A (ja) | 2005-06-30 |
RS68204A (en) | 2007-02-05 |
PE20040188A1 (es) | 2004-05-17 |
ZA200406066B (en) | 2005-06-08 |
EP1474134A1 (de) | 2004-11-10 |
HRP20040702A2 (en) | 2005-04-30 |
AU2003244430A1 (en) | 2003-09-02 |
RU2004126702A (ru) | 2005-04-20 |
PL370488A1 (en) | 2005-05-30 |
HUP0402593A2 (hu) | 2005-04-28 |
NZ534479A (en) | 2006-03-31 |
TW200306850A (en) | 2003-12-01 |
CN1319528C (zh) | 2007-06-06 |
ATE520398T1 (de) | 2011-09-15 |
NO20043698L (no) | 2004-08-31 |
BR0307443A (pt) | 2005-01-04 |
EP1474134B1 (de) | 2011-08-17 |
CN1694697A (zh) | 2005-11-09 |
CO5601009A2 (es) | 2006-01-31 |
JP4733348B2 (ja) | 2011-07-27 |
KR20040083498A (ko) | 2004-10-02 |
CA2474888A1 (en) | 2003-08-14 |
MA27170A1 (fr) | 2005-01-03 |
MXPA04007569A (es) | 2004-11-01 |
AR038387A1 (es) | 2005-01-12 |
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