Clinical Research

Study Endpoints

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Primary Endpoint

  • Change from baseline in SBP and DBP during the last 6 hours of the dosing interval using ambulatory blood pressure monitoring (ABPM)

Secondary Endpoints

  • Change from baseline in SBP and DBP during the last 6 hours of the dosing interval using ABPM
  • Changes in other ABPM-derived parameters
  • Changes in trough cuff SBP and DBP
  • Response rates
  • Changes in health-related quality of life

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