Amorcyte was incorporated in May 2005 and received FDA approval to open a Phase I trial IND for its lead product, AMR-001, in September 2005.
Headquartered in Hackensack, New Jersey, Amorcyte, Inc. is a biopharmaceutical company focusing on the development of cellar therapies to treat cardiovascular disease.
Our initial emphasis will be on acute myocardial infarct. Our lead product is a CD34+ enriched cellular product that has demonstrated significant activity in repairing myocardium after an AMI.
Amorcyte initiated the Phase I trial in January of 2006 at Emory University. The goal of the first phase of this study is to establish the dose potency, identity, efficacy, and safety of AMR-001.