To Evaluate the Safety and Efficacy of MANP in Subjects With Difficult to Control/ Resistant Hypertension
Sponsored by E-Star BioTech, LLC
About this study
This is a Phase 2 dose-titration study designed to evaluate the safety and efficacy of MANP subcutaneous injection compared to placebo in reducing baseline daytime systolic blood pressure (SBP), derived from 24-hour ambulatory blood pressure monitoring (ABPM), in subjects with hypertension who are taking 3 or more antihypertensive medications with different mechanisms of action.
Enrolling at this location
Monroe Biomedical Research
Monroe, North Carolina
I'm interestedThis study also enrolls at 28 other locations. See all.
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Trial data sourced from ClinicalTrials.gov.