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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06343298
Study type Interventional
Source E-Star BioTech, LLC
Contact Seetha R Iyer, MS
Phone 212-271-4295
Email sri@icw.ventures
Status Not yet recruiting
Phase Phase 2
Start date July 1, 2024
Completion date August 1, 2025