drugset / Trial / NCT01495364

NBS10 (Also Known as AMR-001) Versus Placebo Post ST Segment Elevation Myocardial Infarction

NCT01495364 ↗

Phase 2 Completed 195 enrolled Lisata Therapeutics, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will assess the safety and efficacy of intracoronary artery administered autologous bone marrow derived stem cells in subjects post ST segment elevation myocardial infarction (STEMI). This will be assessed by evaluating and comparing the autologous stem cell treatment group to the control group in terms of the occurrence of AE's, SAE's and Major Adverse Cardiac Events (MACE), by the change in myocardial perfusion (RTSS) measured quantitatively by gated single photon emission computed tomography myocardial perfusion imaging (gated SPECT MPI), and other secondary endpoints such as LVEF measured by cardiac MRI in addition to other endpoints.

Timeline

Start
2011-12
Primary completion
2014-06
Completion
2016-04

Outcome

Missed primary endpoint

paper No differences in myocardial perfusion or adverse events were observed between the control and treatment groups PMID 27821724 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject NBS10 Cell therapy 1e+07 cells Other