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Clinical Trial Summary

This is a Phase 2 adaptive, double-blinded, placebo-controlled, randomized, multi-center trial study to evaluate the safety and efficacy of a single dose of AB-1002, administered via antegrade intracoronary artery infusion, in males and females age >18 years with non-ischemic cardiomyopathy and NYHA Class III symptoms of HF. Subjects will be randomized into one of three treatment groups in a 1:1:1


Clinical Trial Description

Subjects will be randomized into one of three treatment groups in a 1:1:1 fashion to either 3.25E13vg (n=30-50), 6.5E13 (n=30-50) or placebo group (n=30-50). Approximately 90 to 150 subjects will be randomly assigned to study intervention Placebo Study duration until the primary analysis at 52 week will be approximately 37 months including 25 months of recruitment and 52-week Observation Period after dosing. Once all the subjects complete the 52 weeks Observation Period, the treatment groups will be unblinded and primary analysis performed. Study participation duration: The study will last 52 weeks from dosing, with another 4 years of long-term follow-up for a total of 5 years. During the 4 year long-term follow up sites will contact subjects twice a year for two years, then once a year for the remaining two years for safety, efficacy assessments, and survival ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05598333
Study type Interventional
Source Asklepios Biopharmaceutical, Inc.
Contact Medical Affairs
Phone (919) 561-6210
Email AskFirst@askbio.com
Status Recruiting
Phase Phase 2
Start date October 20, 2023
Completion date December 2030

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