FDA Grants Fast Track Designation to Cardium Therapeutics, Inc.'s Phase 3 Angiogenic Gene Therapy for Heart Disease

SAN DIEGO--(BUSINESS WIRE)--Cardium Therapeutics (OTCBB:CDTP) announced that the U.S. Food and Drug Administration (FDA) has granted fast track designation to the Company’s lead product candidate, Generx™ (alferminogene tadenovec, Ad5FGF-4) for the potential treatment of myocardial ischemia. Myocardial ischemia, insufficient blood flow within the heart muscle, gives rise to angina associated with coronary heart disease. Generx represents a new therapeutic class of biologics designed to promote angiogenesis, a natural process of blood vessel growth within the heart muscle, following a one-time intracoronary administration from a standard cardiac infusion catheter.
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