Hypertension
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients who were assigned to the CS-3150 group in phase 3 studies (7 studies in total)
Exclusion criteria
Exclusion criteria: Not applicable
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Efficacy endpoint; Change in office sitting BP (systolic BP and diastolic BP) from baseline to Week 12 Safety endpoint; Number of patients with following serum potassium levels (1) 5.5 mEq/L and more (2) 6.0 mEq/L and more, or 5.5 mEq/L and more on two consecutive occasions | — |
Countries
Japan
Contacts
Daiichi Sankyo Co., Ltd. Primary Medical Science Department