Clinical Trials Directory

Trials / Completed

CompletedNCT02432937

Corever in the Treatment of Hypertension

A Double-Blind, Randomized, Placebo-Controlled, Parallel-Group, Phase III Study of Corever for the Treatment of Hypertension

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
134 (actual)
Sponsor
TSH Biopharm Corporation Limited · Industry
Sex
All
Age
20 Years – 90 Years
Healthy volunteers
Not accepted

Summary

The study primarily aims to compare the effects of two doses of Corever with placebo in patients with hypertension.

Detailed description

The study aims to compare the effects of two doses of Corever with placebo in patients with essential hypertension. Eligible subjects who belong to one of the following subtypes are planned to be enrolled: (1) patients with essential hypertension without drug control, or (2) uncontrolled hypertension despite treatment with up to 2 antihypertensive agents. Of note, the second category will receive randomized study treatments in addition to continuing their previous medication throughout the trial. The study also wants to investigate the safety profile of Corever during treatment period.

Conditions

Interventions

TypeNameDescription
DRUGCoreverCorever

Timeline

Start date
2015-01-01
Primary completion
2016-06-01
Completion
2016-08-01
First posted
2015-05-04
Last updated
2016-11-04

Locations

8 sites across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT02432937. Inclusion in this directory is not an endorsement.