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CLINICAL TRIALS PROFILE FOR MOEXIPRIL HYDROCHLORIDE
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All Clinical Trials for Moexipril Hydrochloride
Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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NCT00588302 | Moexipril for Primary Biliary Cirrhosis | Completed | UCB Pharma | Phase 2 | 2003-06-01 | The blockade of angiotensin II synthesis attenuates hepatic fibrosis in different experimental models of chronic liver injury. We aimed to determine the safety and efficacy of moexipril, an angiotensin-converting enzyme (ACE) inhibitor, on liver biochemistries, Mayo risk score, and health-related quality of life in patients with primary biliary cirrhosis (PBC) who have had a suboptimal response to ursodeoxycholic acid (UDCA). |
NCT00588302 | Moexipril for Primary Biliary Cirrhosis | Completed | Mayo Clinic | Phase 2 | 2003-06-01 | The blockade of angiotensin II synthesis attenuates hepatic fibrosis in different experimental models of chronic liver injury. We aimed to determine the safety and efficacy of moexipril, an angiotensin-converting enzyme (ACE) inhibitor, on liver biochemistries, Mayo risk score, and health-related quality of life in patients with primary biliary cirrhosis (PBC) who have had a suboptimal response to ursodeoxycholic acid (UDCA). |
NCT00834067 | Moexipril HCl/Hydrochlorothiazide 15/25 mg Tablets Under Non-Fasting Conditions | Completed | Teva Pharmaceuticals USA | Phase 1 | 2003-10-01 | The objective of this study is to compare the relative bioavailability of moexipril HCl/ hydrochlorothiazide 15/25 mg tablets (manufactured and distributed by TEVA Pharmaceuticals USA) with that of UNIRETIC® 15/25 mg tablets (Schwartz Pharma) in healthy, adult, non-smoking subjects under non-fasting conditions. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
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