A Phase II Randomised Double-Blind Placebo-Controlled Study of the Efficacy Safety and Tolerability of Oral NP202 in Adults who have Left Ventricular Systolic Dysfunction following Myocardial Infarction.
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- STATUS
- Not Recruiting
Updated on 19 February 2024
Summary
The purpose of this study is to evaluate the efficacy of NP202 compared to placebo, when administered once daily for 3 months, in attenuating pathological left ventricular remodeling in patients post myocardial infarction.
Description
The purpose of this study is to evaluate the efficacy of NP202 compared to placebo, when administered once daily for 3 months, in attenuating pathological left ventricular remodeling in patients post myocardial infarction.
Details
| Condition | myocardial infarction |
|---|---|
| Age | 100years or below |
| Clinical Study Identifier | TX5943 |
| Last Modified on | 19 February 2024 |
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