Clinical trial
A Phase-3 Randomized, Double-Blind, Parallel-Group Efficacy and Safety Study Evaluating the Fixed-Dose Combination of Candesartan Plus Amlodipine (8/5 mg) in Chinese Subjects With Mild/Moderate Essential Hypertension, Who Do Not Achieve Target Blood Pressure Following Treatment With Amlodipine 5 mg Monotherapy
NCT02969265 is registered in ClinicalTrials.gov with Takeda as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase-3 Randomized, Double-Blind, Parallel-Group Efficacy and Safety Study Evaluating the Fixed-Dose Combination of Candesartan Plus Amlodipine (8/5 mg) in Chinese Subjects With Mild/Moderate Essential Hypertension, Who Do Not Achieve Target Blood Pressure Following Treatment With Amlodipine 5 mg Monotherapy
- Lead sponsor
- Takeda
- Phase
- Phase 3
- Overall status
- Withdrawn
- Start date
- May 9, 2017
- Completion date
- July 26, 2018
- Enrollment
- 0 (actual)
- Sites
- 25
Conditions
As the registry lists them; a condition with its own page is linked.