JP2004520268A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2004520268A5 JP2004520268A5 JP2002520812A JP2002520812A JP2004520268A5 JP 2004520268 A5 JP2004520268 A5 JP 2004520268A5 JP 2002520812 A JP2002520812 A JP 2002520812A JP 2002520812 A JP2002520812 A JP 2002520812A JP 2004520268 A5 JP2004520268 A5 JP 2004520268A5
- Authority
- JP
- Japan
- Prior art keywords
- ang
- antagonist
- ace inhibitor
- ramipril
- pharmaceutical composition
- 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.)
- Pending
Links
- 239000005541 ACE inhibitor Substances 0.000 description 18
- 229940044094 angiotensin-converting-enzyme inhibitor Drugs 0.000 description 18
- 239000005557 antagonist Substances 0.000 description 18
- RMMXLENWKUUMAY-UHFFFAOYSA-N telmisartan Chemical compound CCCC1=NC2=C(C)C=C(C=3N(C4=CC=CC=C4N=3)C)C=C2N1CC(C=C1)=CC=C1C1=CC=CC=C1C(O)=O RMMXLENWKUUMAY-UHFFFAOYSA-N 0.000 description 18
- 238000000034 method Methods 0.000 description 13
- 239000008194 pharmaceutical composition Substances 0.000 description 10
- 229960003401 ramipril Drugs 0.000 description 10
- HDACQVRGBOVJII-JBDAPHQKSA-N ramipril Chemical compound C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](C[C@@H]2CCC[C@@H]21)C(O)=O)CC1=CC=CC=C1 HDACQVRGBOVJII-JBDAPHQKSA-N 0.000 description 10
- 239000005537 C09CA07 - Telmisartan Substances 0.000 description 9
- 229960005187 telmisartan Drugs 0.000 description 9
- 230000002265 prevention Effects 0.000 description 5
- 108010007859 Lisinopril Proteins 0.000 description 4
- 229960002394 lisinopril Drugs 0.000 description 4
- RLAWWYSOJDYHDC-BZSNNMDCSA-N lisinopril Chemical compound C([C@H](N[C@@H](CCCCN)C(=O)N1[C@@H](CCC1)C(O)=O)C(O)=O)CC1=CC=CC=C1 RLAWWYSOJDYHDC-BZSNNMDCSA-N 0.000 description 4
- BIDNLKIUORFRQP-XYGFDPSESA-N (2s,4s)-4-cyclohexyl-1-[2-[[(1s)-2-methyl-1-propanoyloxypropoxy]-(4-phenylbutyl)phosphoryl]acetyl]pyrrolidine-2-carboxylic acid Chemical compound C([P@@](=O)(O[C@H](OC(=O)CC)C(C)C)CC(=O)N1[C@@H](C[C@H](C1)C1CCCCC1)C(O)=O)CCCC1=CC=CC=C1 BIDNLKIUORFRQP-XYGFDPSESA-N 0.000 description 3
- XPCFTKFZXHTYIP-PMACEKPBSA-N Benazepril Chemical group C([C@@H](C(=O)OCC)N[C@@H]1C(N(CC(O)=O)C2=CC=CC=C2CC1)=O)CC1=CC=CC=C1 XPCFTKFZXHTYIP-PMACEKPBSA-N 0.000 description 3
- 239000002083 C09CA01 - Losartan Substances 0.000 description 3
- 206010007559 Cardiac failure congestive Diseases 0.000 description 3
- 108010061435 Enalapril Proteins 0.000 description 3
- 206010019280 Heart failures Diseases 0.000 description 3
- 206010020772 Hypertension Diseases 0.000 description 3
- UWWDHYUMIORJTA-HSQYWUDLSA-N Moexipril Chemical compound C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](CC2=CC(OC)=C(OC)C=C2C1)C(O)=O)CC1=CC=CC=C1 UWWDHYUMIORJTA-HSQYWUDLSA-N 0.000 description 3
- VXFJYXUZANRPDJ-WTNASJBWSA-N Trandopril Chemical compound C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](C[C@H]2CCCC[C@@H]21)C(O)=O)CC1=CC=CC=C1 VXFJYXUZANRPDJ-WTNASJBWSA-N 0.000 description 3
- 229960004530 benazepril Drugs 0.000 description 3
- 229960000830 captopril Drugs 0.000 description 3
- FAKRSMQSSFJEIM-RQJHMYQMSA-N captopril Chemical compound SC[C@@H](C)C(=O)N1CCC[C@H]1C(O)=O FAKRSMQSSFJEIM-RQJHMYQMSA-N 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 230000002526 effect on cardiovascular system Effects 0.000 description 3
- 229960000873 enalapril Drugs 0.000 description 3
- GBXSMTUPTTWBMN-XIRDDKMYSA-N enalapril Chemical compound C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](CCC1)C(O)=O)CC1=CC=CC=C1 GBXSMTUPTTWBMN-XIRDDKMYSA-N 0.000 description 3
- 229960002490 fosinopril Drugs 0.000 description 3
- 229960001195 imidapril Drugs 0.000 description 3
- KLZWOWYOHUKJIG-BPUTZDHNSA-N imidapril Chemical compound C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1C(N(C)C[C@H]1C(O)=O)=O)CC1=CC=CC=C1 KLZWOWYOHUKJIG-BPUTZDHNSA-N 0.000 description 3
- 229960004773 losartan Drugs 0.000 description 3
- KJJZZJSZUJXYEA-UHFFFAOYSA-N losartan Chemical compound CCCCC1=NC(Cl)=C(CO)N1CC1=CC=C(C=2C(=CC=CC=2)C=2[N]N=NN=2)C=C1 KJJZZJSZUJXYEA-UHFFFAOYSA-N 0.000 description 3
- 230000001404 mediated effect Effects 0.000 description 3
- 229960005170 moexipril Drugs 0.000 description 3
- 229960001455 quinapril Drugs 0.000 description 3
- JSDRRTOADPPCHY-HSQYWUDLSA-N quinapril Chemical compound C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](CC2=CC=CC=C2C1)C(O)=O)CC1=CC=CC=C1 JSDRRTOADPPCHY-HSQYWUDLSA-N 0.000 description 3
- 102000005962 receptors Human genes 0.000 description 3
- 108020003175 receptors Proteins 0.000 description 3
- 229960002051 trandolapril Drugs 0.000 description 3
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 description 2
- 239000002080 C09CA02 - Eprosartan Substances 0.000 description 2
- 239000004072 C09CA03 - Valsartan Substances 0.000 description 2
- 239000002947 C09CA04 - Irbesartan Substances 0.000 description 2
- 239000002053 C09CA06 - Candesartan Substances 0.000 description 2
- 206010010904 Convulsion Diseases 0.000 description 2
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 2
- 208000013616 Respiratory Distress Syndrome Diseases 0.000 description 2
- 206010000891 acute myocardial infarction Diseases 0.000 description 2
- 208000011341 adult acute respiratory distress syndrome Diseases 0.000 description 2
- 201000000028 adult respiratory distress syndrome Diseases 0.000 description 2
- 206010006451 bronchitis Diseases 0.000 description 2
- 229960000932 candesartan Drugs 0.000 description 2
- SGZAIDDFHDDFJU-UHFFFAOYSA-N candesartan Chemical compound CCOC1=NC2=CC=CC(C(O)=O)=C2N1CC(C=C1)=CC=C1C1=CC=CC=C1C1=NN=N[N]1 SGZAIDDFHDDFJU-UHFFFAOYSA-N 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 229960004563 eprosartan Drugs 0.000 description 2
- OROAFUQRIXKEMV-LDADJPATSA-N eprosartan Chemical compound C=1C=C(C(O)=O)C=CC=1CN1C(CCCC)=NC=C1\C=C(C(O)=O)/CC1=CC=CS1 OROAFUQRIXKEMV-LDADJPATSA-N 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 229960002198 irbesartan Drugs 0.000 description 2
- YCPOHTHPUREGFM-UHFFFAOYSA-N irbesartan Chemical compound O=C1N(CC=2C=CC(=CC=2)C=2C(=CC=CC=2)C=2[N]N=NN=2)C(CCCC)=NC21CCCC2 YCPOHTHPUREGFM-UHFFFAOYSA-N 0.000 description 2
- 201000005202 lung cancer Diseases 0.000 description 2
- 208000020816 lung neoplasm Diseases 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000007911 parenteral administration Methods 0.000 description 2
- 229960002582 perindopril Drugs 0.000 description 2
- IPVQLZZIHOAWMC-QXKUPLGCSA-N perindopril Chemical compound C1CCC[C@H]2C[C@@H](C(O)=O)N(C(=O)[C@H](C)N[C@@H](CCC)C(=O)OCC)[C@H]21 IPVQLZZIHOAWMC-QXKUPLGCSA-N 0.000 description 2
- 230000002685 pulmonary effect Effects 0.000 description 2
- 230000008733 trauma Effects 0.000 description 2
- 229960004699 valsartan Drugs 0.000 description 2
- SJSNUMAYCRRIOM-QFIPXVFZSA-N valsartan Chemical compound C1=CC(CN(C(=O)CCCC)[C@@H](C(C)C)C(O)=O)=CC=C1C1=CC=CC=C1C1=NN=N[N]1 SJSNUMAYCRRIOM-QFIPXVFZSA-N 0.000 description 2
- 230000002792 vascular Effects 0.000 description 2
- 208000017612 Acute Hemorrhagic Pancreatitis Diseases 0.000 description 1
- 206010002383 Angina Pectoris Diseases 0.000 description 1
- 102000005862 Angiotensin II Human genes 0.000 description 1
- 101800000733 Angiotensin-2 Proteins 0.000 description 1
- 206010051113 Arterial restenosis Diseases 0.000 description 1
- 206010003210 Arteriosclerosis Diseases 0.000 description 1
- 201000001320 Atherosclerosis Diseases 0.000 description 1
- 208000037260 Atherosclerotic Plaque Diseases 0.000 description 1
- 101800004538 Bradykinin Proteins 0.000 description 1
- 102400000967 Bradykinin Human genes 0.000 description 1
- 206010006187 Breast cancer Diseases 0.000 description 1
- 208000026310 Breast neoplasm Diseases 0.000 description 1
- 206010006458 Bronchitis chronic Diseases 0.000 description 1
- 239000002081 C09CA05 - Tasosartan Substances 0.000 description 1
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 201000003883 Cystic fibrosis Diseases 0.000 description 1
- 208000007342 Diabetic Nephropathies Diseases 0.000 description 1
- 208000013600 Diabetic vascular disease Diseases 0.000 description 1
- 206010014561 Emphysema Diseases 0.000 description 1
- 208000003241 Fat Embolism Diseases 0.000 description 1
- QXZGBUJJYSLZLT-UHFFFAOYSA-N H-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg-OH Natural products NC(N)=NCCCC(N)C(=O)N1CCCC1C(=O)N1C(C(=O)NCC(=O)NC(CC=2C=CC=CC=2)C(=O)NC(CO)C(=O)N2C(CCC2)C(=O)NC(CC=2C=CC=CC=2)C(=O)NC(CCCN=C(N)N)C(O)=O)CCC1 QXZGBUJJYSLZLT-UHFFFAOYSA-N 0.000 description 1
- CZGUSIXMZVURDU-JZXHSEFVSA-N Ile(5)-angiotensin II Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC=1C=CC=CC=1)C([O-])=O)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=[NH2+])NC(=O)[C@@H]([NH3+])CC([O-])=O)C(C)C)C1=CC=C(O)C=C1 CZGUSIXMZVURDU-JZXHSEFVSA-N 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 208000029523 Interstitial Lung disease Diseases 0.000 description 1
- 208000007177 Left Ventricular Hypertrophy Diseases 0.000 description 1
- 239000005480 Olmesartan Substances 0.000 description 1
- 206010033650 Pancreatitis haemorrhagic Diseases 0.000 description 1
- 206010035664 Pneumonia Diseases 0.000 description 1
- 206010053879 Sepsis syndrome Diseases 0.000 description 1
- 206010051379 Systemic Inflammatory Response Syndrome Diseases 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000002399 angioplasty Methods 0.000 description 1
- 229950006323 angiotensin ii Drugs 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- QXZGBUJJYSLZLT-FDISYFBBSA-N bradykinin Chemical compound NC(=N)NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(=O)NCC(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CO)C(=O)N2[C@@H](CCC2)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)CCC1 QXZGBUJJYSLZLT-FDISYFBBSA-N 0.000 description 1
- 230000000747 cardiac effect Effects 0.000 description 1
- 230000002612 cardiopulmonary effect Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000004663 cell proliferation Effects 0.000 description 1
- 210000000038 chest Anatomy 0.000 description 1
- 208000007451 chronic bronchitis Diseases 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 201000009101 diabetic angiopathy Diseases 0.000 description 1
- 208000033679 diabetic kidney disease Diseases 0.000 description 1
- 201000002249 diabetic peripheral angiopathy Diseases 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 230000004064 dysfunction Effects 0.000 description 1
- 210000002919 epithelial cell Anatomy 0.000 description 1
- 230000008508 epithelial proliferation Effects 0.000 description 1
- 210000000981 epithelium Anatomy 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 206010020718 hyperplasia Diseases 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 210000002570 interstitial cell Anatomy 0.000 description 1
- 230000000302 ischemic effect Effects 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 208000010125 myocardial infarction Diseases 0.000 description 1
- 208000031225 myocardial ischemia Diseases 0.000 description 1
- 230000000414 obstructive effect Effects 0.000 description 1
- 229960005117 olmesartan Drugs 0.000 description 1
- VTRAEEWXHOVJFV-UHFFFAOYSA-N olmesartan Chemical compound CCCC1=NC(C(C)(C)O)=C(C(O)=O)N1CC1=CC=C(C=2C(=CC=CC=2)C=2NN=NN=2)C=C1 VTRAEEWXHOVJFV-UHFFFAOYSA-N 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- 208000023504 respiratory system disease Diseases 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229960000651 tasosartan Drugs 0.000 description 1
- ADXGNEYLLLSOAR-UHFFFAOYSA-N tasosartan Chemical compound C12=NC(C)=NC(C)=C2CCC(=O)N1CC(C=C1)=CC=C1C1=CC=CC=C1C=1N=NNN=1 ADXGNEYLLLSOAR-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000007631 vascular surgery Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0020691.2A GB0020691D0 (en) | 2000-08-22 | 2000-08-22 | Pharmaceutical combination |
| DE10108215A DE10108215A1 (de) | 2000-08-22 | 2001-02-20 | Pharmazeutische Kombination von Antagonisten von Angiotensin II und Hemmern von Angiotensin II konvertierendem Enzym |
| PCT/EP2001/009428 WO2002015891A2 (en) | 2000-08-22 | 2001-08-16 | Pharmaceutical combination of angiotensin ii antagonists and ace inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004520268A JP2004520268A (ja) | 2004-07-08 |
| JP2004520268A5 true JP2004520268A5 (enExample) | 2008-10-02 |
Family
ID=32327460
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002520812A Pending JP2004520268A (ja) | 2000-08-22 | 2001-08-16 | アンギオテンシンｉｉ拮抗剤とアンギオテンシンｉ変換酵素阻害剤とを含有する医薬組成物 |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US20060154976A1 (enExample) |
| EP (1) | EP1671632A1 (enExample) |
| JP (1) | JP2004520268A (enExample) |
| KR (1) | KR20030064383A (enExample) |
| AR (1) | AR030468A1 (enExample) |
| EA (1) | EA200300224A1 (enExample) |
| EE (1) | EE200300075A (enExample) |
| HR (1) | HRP20030124A2 (enExample) |
| HU (1) | HUP0303836A2 (enExample) |
| MX (1) | MXPA03001509A (enExample) |
| NZ (1) | NZ546884A (enExample) |
| PL (1) | PL366419A1 (enExample) |
| SG (1) | SG148838A1 (enExample) |
| TW (1) | TWI281858B (enExample) |
| UY (1) | UY26893A1 (enExample) |
| YU (1) | YU12703A (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004008804A1 (de) * | 2004-02-20 | 2005-09-08 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Mehrschichttablette |
| CN116120280A (zh) * | 2021-11-12 | 2023-05-16 | 成都贝诺科成生物科技有限公司 | 一种电荷平衡的复合物、其制备方法及其用途 |
| CN116115763A (zh) * | 2021-11-12 | 2023-05-16 | 成都贝诺科成生物科技有限公司 | 一种含有h1组胺受体拮抗剂的联合用药物 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5821232A (en) * | 1990-05-11 | 1998-10-13 | Pfizer Inc. | Synergistic therapeutic compositions and methods |
| EP0629408A1 (en) * | 1993-06-16 | 1994-12-21 | LABORATOIRES MERCK, SHARP & DOHME-CHIBRET | Combination of angiotensin converting enzyme inhibitors and AII antagonists |
| US6063911A (en) * | 1993-12-01 | 2000-05-16 | Marine Polymer Technologies, Inc. | Methods and compositions for treatment of cell proliferative disorders |
| MX9707683A (es) * | 1995-04-07 | 1997-12-31 | Novartis Ag | Composiciones de combinacion que contienen benazepril o benazeprilat y valsartan. |
| WO1997002032A1 (en) * | 1995-06-30 | 1997-01-23 | Merck & Co., Inc. | Method of treating renal disease using an ace inhibitor and an aii antagonist |
| DE69712338T2 (de) * | 1996-06-24 | 2002-11-07 | Merck & Co., Inc. | Zusammensetzung auf basis von enalapril und losartan |
| GB9801398D0 (en) * | 1998-01-22 | 1998-03-18 | Anggard Erik E | Chemical compounds |
| US6326379B1 (en) * | 1998-09-16 | 2001-12-04 | Bristol-Myers Squibb Co. | Fused pyridine inhibitors of cGMP phosphodiesterase |
| US20040009952A1 (en) * | 1998-10-19 | 2004-01-15 | Giovanni Gambaro | TGF-beta gene overexpression preventing substances for the treatment of disorders connected with pathological overexpression of TGF-beta |
| US6465502B1 (en) * | 1998-12-23 | 2002-10-15 | Novartis Ag | Additional therapeutic use |
| EP1013273A1 (en) * | 1998-12-23 | 2000-06-28 | Novartis AG | Use of AT-1 receptor antagonist or AT-2 receptor modulator for treating diseases associated with an increase of AT-1 or AT-2 receptors |
| EE05670B1 (et) * | 1999-08-30 | 2013-08-15 | Aventis Pharma Deutschland Gmbh | Ramipriil kardiovaskulaarsete haigusjuhtude rahoidmiseks |
-
2001
- 2001-08-16 PL PL01366419A patent/PL366419A1/xx not_active Application Discontinuation
- 2001-08-16 JP JP2002520812A patent/JP2004520268A/ja active Pending
- 2001-08-16 EP EP06000777A patent/EP1671632A1/en not_active Ceased
- 2001-08-16 NZ NZ546884A patent/NZ546884A/en unknown
- 2001-08-16 MX MXPA03001509A patent/MXPA03001509A/es not_active Application Discontinuation
- 2001-08-16 YU YU12703A patent/YU12703A/sh unknown
- 2001-08-16 EA EA200300224A patent/EA200300224A1/ru unknown
- 2001-08-16 HU HU0303836A patent/HUP0303836A2/hu unknown
- 2001-08-16 SG SG200501008-7A patent/SG148838A1/en unknown
- 2001-08-16 UY UY26893A patent/UY26893A1/es not_active Application Discontinuation
- 2001-08-16 HR HR20030124A patent/HRP20030124A2/hr not_active Application Discontinuation
- 2001-08-16 EE EEP200300075A patent/EE200300075A/xx unknown
- 2001-08-16 KR KR10-2003-7002476A patent/KR20030064383A/ko not_active Ceased
- 2001-08-20 TW TW090120386A patent/TWI281858B/zh not_active IP Right Cessation
- 2001-08-22 AR ARP010104001A patent/AR030468A1/es unknown
-
2006
- 2006-03-15 US US11/375,836 patent/US20060154976A1/en not_active Abandoned
-
2008
- 2008-02-21 US US12/035,166 patent/US20080146639A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2001295465B2 (en) | Pharmaceutical combination of angiotensin II antagonists and ace inhibitors | |
| JPWO2003018061A1 (ja) | キマーゼ阻害剤及びａｃｅ阻害剤を有効成分として含有する薬剤 | |
| EP3027183B1 (en) | Selective at2 receptor agonists for use in treatment of cachexia | |
| AU2001295465A1 (en) | Pharmaceutical combination of angiotensin II antagonists and ace inhibitors | |
| CN104780942A (zh) | Sglt2抑制剂和抗高血压药的组合 | |
| CA2755543A1 (en) | Compositions and methods for treatment and prevention of cardiovascular disease | |
| Di Daniele | Therapeutic approaches of uncomplicated arterial hypertension in patients with COPD | |
| AU6291696A (en) | Method of treating renal disease using an ace inhibitor and an A II antagonist | |
| JP2004520268A5 (enExample) | ||
| EP3090744B1 (en) | Pharmaceutical complex formulation comprising angiotensin ii receptor blocker and hmg-coa reductase inhibitor | |
| CN1187050C (zh) | 内皮素拮抗剂和血管紧张肽原酶－血管紧张肽系统抑制剂的联合体系 | |
| US20080146639A1 (en) | Pharmaceutical Combination of Angiotensin II Antagonists and Angiotensin I Converting Enzyme Inhibitors | |
| WO2004098611A1 (ja) | 増強剤 | |
| CN104324377A (zh) | 一种复方降压制剂及其应用 | |
| JP2007314568A (ja) | チオベンズイミダゾール誘導体 | |
| US20080275011A1 (en) | Use of dipyridamole, acetylsalicylic acid and an angiotensin ii antagonist for treatment and prevention of vascular events | |
| KR20050018330A (ko) | 혈관장애의 치료 및 예방을 위한 디피리다몰,아세틸살리실산 및 안지오텐신 ⅱ 길항제의 용도 | |
| White et al. | THE NEW ANGIOTENSIN RECEPTOR BLOCKER AZILSARTAN MEDOXOMIL HAS SIGNIFICANTLY GREATER 24-HOUR BLOOD PRESSURE LOWERING EFFICACY TO BOTH OLMESARTAN AND VALSARTAN: 9D. 05 | |
| Krämer et al. | THE NON-PEPTIDE AT2-RECEPTOR AGONIST COMPOUND 21 AMELIORATES HYPERTROPHY AND FIBROSIS IN UREMIA-ASSOCIATED CARDIOMYOPATHY: 9D. 04 | |
| ZA200300556B (en) | Pharmaceutical combination of angiotensin II antagonists and ace inhibitors. | |
| Tiwaskar | End organ protection | |
| HK1104976A (en) | Pharmaceutical combination of angiotensin ii antagonists and angiotensin i converting enzyme inhibitors | |
| HK1057487A (en) | Pharmaceutical combination of angiotensin ii antagonists and angiotensin i converting enzyme inhibitors | |
| AU2003235004A1 (en) | Use of dipyridamole, acetylsalicylic acid and an angiotensin II antagonist for treatment and prevention of vascular events | |
| AU2007237280A1 (en) | Pharmaceutical combination of Angiotensin II antagonists and Angiotensin I converting enzyme inhibitors |