Essential hypertensive patients with stable angina and dyslipidemia
Conditions
Interventions
investigational material(s)
Generic name etc : Azilsartan (Proprietary name: Azilva)
INN of investigational material :
Therapeutic category code : 214 Antihypertensives
Dosage and Administration for
Sponsors
TAKEDA PHARMACEUTICAL COMPANY LTD.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Patients with essential hypertension with office blood pressure before the start of study treatment (Week 0) meeting the following criteria who are appropriate for azilsartan therapy in the opinion of the principal investigator or investigator - Patients aged >= 75 years at the time of informed consent: Sitting systolic blood pressure >= 150 mmHg or sitting diastolic blood pressure >= 90 mmHg - Patients aged = 130 mmHg or sitting diastolic blood pressure >= 80 mmHg - Patients aged = 130 mmHg or sitting diastolic blood pressure >= 80 mmHg - Patients meeting none of the above: Sitting systolic blood pressure >= 140 mmHg or sitting diastolic blood pressure >= 90 mmHg 2.Patients with stable angina with a coronary stenosis confirmed by coronary angiography who are planned to undergo percutaneous coronary intervention with stent placement (any type of stent) 3.Patients with findings of integrated backscatter intravascular ultrasound (IB-IVUS) to be performed before the start of study treatment (Week 0) showing plaque at >= 5 mm proximal to the proximal end of the inserted stent in the coronary artery 4.Patients with dyslipidemia meeting both of the following criteria: - Patients treated with one HMG-CoA reductase inhibitor with no change in the dosage for at least 12 weeks before informed consent - Patients with an LDL-C level of < 100 mg/dL as shown by a laboratory test performed within 4 weeks before informed consent 5.Men or women aged 20 or older at the time of informed consent 6.Patients capable of making outpatient study visits throughout the observation period 7.Patients who, in the opinion of the principal investigator or investigator, are capable of understanding the contents of the clinical study and complying with the study requirements 8.Patients capable of providing written consent in person before any study procedures
Exclusion criteria
Exclusion criteria: 1.Patients with secondary hypertension or malignant hypertension 2.Patients who took any renin-angiotensin system inhibitor within 12 weeks before informed consent 3.Patients who previously underwent coronary artery bypass grafting 4.Patients with type 1 diabetes mellitus 5.Patients with insulin therapy 6.Patients with an HbA1c level (National Glycohemoglobin Standardization Program [NGSP] value) of >= 7.0% as shown by a laboratory test performed within 4 weeks before informed consent 7.Patients with the plaque unevaluable because of severe calcification of the coronary artery shown by IB-IVUS to be performed before the start of study treatment (Week 0) 8.Patients with a change to their antidyslipidemic medication (including a change to the dosage) within 12 weeks before informed consent 9.Patients with clinically evident renal disorder (defined as eGFR = 5.5 mEq/L) 12.Patients with a history of hypersensitivity or allergy to azilsartan 13.Patients participating in any other clinical study 14.Pregnant women, women with possible pregnancy, or breastfeeding women 15.Other patients who are inappropriate for participation in this study in the opinion of the principal investigator or investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in percentage of the lipid pool in the coronary artery plaque Primary timeframe: 32 weeks Change in percentage of the lipid pool in the coronary artery plaque from the start of the treatment period at the end of the treatment period (Week 32). Percentage of the lipid pool in the coronary artery plaque is measured by integrated backscatter intravascular ultrasound (IB-IVUS). | — |
Secondary
| Measure | Time frame |
|---|---|
| - Change in volume of the coronary artery plaque - Change in percentage of the fibrotic component in the coronary artery plaque - Change in percentage of the calcified component in the coronary artery plaque - Change in number of microchannels - Change in thickness of the fibrous cap Secondary timeframe: 32 weeks Each outcome change from the start of the treatment period to the end of the treatment period. Each outcome is measured by integrated backscatter intravascular ultrasound (IB-IVUS) or Optical Coherence Tomography (OCT). | — |
Outcome results
None listed