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Efficacy and Safety of Irbesartan and Atorvastatin in Hypertension and Hyperlipidemia

Phase 3
Completed
Conditions
Hypertension
Hyperlipidemia
Interventions
Drug: Irbesartan/Atorvastatin A
Drug: Placebo
Drug: Irbesartan/Atorvastatin B
Registration Number
NCT01442987
Lead Sponsor
Hanmi Pharmaceutical Company Limited
Brief Summary

The purpose of this study is to evaluate efficacy and safety of coadministered Irbesartan and Atorvastatin in patients with hypertension and hyperlipidemia.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
230
Inclusion Criteria
  • Aged between 19 and 75 years
  • Signed informed consent
Exclusion Criteria
  • At screening, SPB ≥ 180mmHg or DBP ≥ 110mmHg or LDL-C > 250mg/dL or TG ≥ 400mg/dL
  • Has a history of hypersensitivity to Angiotensin Ⅱ receptor blocker or HMG-CoA reductase inhibitor or component of this drug
  • Has a history of multi-drug allergy

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
Irbesartan/Atorvastatin AIrbesartan/Atorvastatin A-
Atorvastatin AAtorvastatin A-
PlaceboPlacebo-
Irbesartan/Atorvastatin BIrbesartan/Atorvastatin B-
Atorvastatin BAtorvastatin B-
IrbesartanIrbesartan-
Primary Outcome Measures
NameTimeMethod
Percent change from baseline to 8 week in LDL-Cholesterolbaseline and 8 week
Change from baseline to 8 week in Blood Pressure.baseline and 8 week
Secondary Outcome Measures
NameTimeMethod
Percentage of patients reaching treatment goals according to NCEP ATP III Guideline and Blood pressure responder rate according to JNC VII Guideline.week 8

Trial Locations

Locations (1)

16 institutions including Seoul National University Hospital

🇰🇷

Seoul, Korea, Republic of

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