Phase 3Completed

Fimasartan/Amlodipine Combination Phase III

A Randomized, Double-blind Multicenter, Phase III Study to Evaluate the Efficacy and Safety of Combination of Fimasartan/Amlodipine Versus Fimasartan Monotherapy in Patients With Essential Hypertension Who Fail to Respond Adequately to Fimasartan Monotherapy.

Sponsor
Boryung Pharmaceutical Co., Ltd (Industry)
Enrollment
143 enrolled
Conditions
Essential Hypertension
Interventions
Fimasartan and Amlodipine; Fimasartan
Ages
adults, older adults
Registry
NCT02152306

Full record on ClinicalTrials.gov

From the registry

The aim of this study is to ensure the superiority of Fimasartan/Amlodipine combination in hypotensive effect after 8 weeks of treatment over Fimasartan monotherapy in patients with hypertension who have no response to Fimasartan 60mg monotherapy.

Primary outcomes

  • Change of Sitting Systolic Blood Pressure(SiSBP) at week 8 of Investigational Product(IP) Administration from the Baseline

History

  1. Last registry update

  2. Study completion

  3. Primary completion

  4. Registered

  5. Started