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Clinical Trial Summary

The main objective of the study will be to assess the efficacy and safety of Allisartan Isoproxil/Amlodipine (240 mg /5 mg) in patients with mild to moderate essential hypertension uncontrolled after 4-week treatment with Amlodipine besylate(5 mg) or Allisartan Isoproxil (240 mg) .


Clinical Trial Description

Amlodipine belongs to the calcium channel blocker (CCB) class of drugs, which acts as antihypertensive agent mainly via blocking calcium channels on the vascular smooth muscle cells to dilate blood vessels. Allisartan Isoproxil belongs to the ARB class of drugs,which can effectively exert antihypertensive effect. The combination of dihydropyridine CCBs and ARBs exerts synergistic antihypertensive effects. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06465264
Study type Interventional
Source Shenzhen Salubris Pharmaceuticals Co., Ltd.
Contact
Status Completed
Phase Phase 3
Start date April 29, 2021
Completion date February 24, 2023

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