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An Efficacy and Safety Study Evaluating the Fixed-Dose Combination of Candesartan Plus Amlodipine in Participants With Mild/Moderate Essential Hypertension
The purpose of this study is to evaluate the efficacy and safety of TCV-116CCB (candesartan cilexetil and amlodipine besylate fixed-dose combination) in Chinese participants with mild to moderate hypertension who do not reach target blood pressure following 4 weeks of treatment with amlodipine monotherapy.
Details
| Lead sponsor | Takeda |
|---|---|
| Phase | PHASE3 |
| Status | WITHDRAWN |
| Start date | Tue May 09 2017 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Thu Jul 26 2018 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Hypertension
Interventions
- Amlodipine
- TCV-116CCB
- Amlodipine Placebo
- TCV-116CCB Placebo
Countries
China