Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07509801

A Study to Evaluate the Safety and Efficacy of NT-88

A Randomized, Single-center, Blinded Analysis Clinical Study to Evaluate the Safety and Efficacy of NT-88 in Patients With Heart Failure With Chronic Mildly Reduced Ejection Fraction

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Guangzhou Manjing biomedicine technology co., ltd · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

A study to evaluate the safety and preliminary efficacy of Zuozhu Daxi in patients with chronic heart failure with mildly reduced ejection fraction

Detailed description

A randomized, single-center, blinded analysis clinical study to evaluate the safety and efficacy of NT-88 inpatients with heart failure with chronic mildly reduced ejection fraction. To evaluate the safety and preliminary efficacy of Zuozhu Daxi in patients with chronic heart failure with mildly reduced ejection fraction

Conditions

Interventions

TypeNameDescription
DRUGConventional therapeutic drugsConventional therapeutic drugs
DRUGNT-88Conventional therapeutic drugs+NT-88

Timeline

Start date
2026-03-30
Primary completion
2027-02-25
Completion
2027-06-30
First posted
2026-04-03
Last updated
2026-04-03

Source: ClinicalTrials.gov record NCT07509801. Inclusion in this directory is not an endorsement.