BioCardia Announces Two Scientific Abstracts Have Been Accepted at the 2024 Technology and Heart Failure Therapeutics Conference - Seite 2

As previously reported, the CardiALLO Heart Failure study follows the Company’s earlier co-sponsored clinical studies of allogeneic mesenchymal stem cells for patients with ischemic heart failure of reduced ejection fraction. This scientific presentation will provide details on the early safety experience from this ongoing clinical study.

“BioCardia is pleased to share these analyses of its ongoing clinical autologous and allogeneic cell therapy studies at the THT Conference,” said Dr. Peter Altman, BioCardia Chief Executive Officer and President. “The positive results in these two development efforts as previously reported have included reduced mortality, enhanced heart function, and improved quality of life with no significant safety concerns with either of these cell therapy product candidates. Both cell therapy candidates are delivered with our proprietary minimally invasive Helix transendocardial biotherapeutic delivery system which is approved for use in Europe and approved for investigational use in the United States. Cell therapies with the unique profiles we are advancing in both the CardiAMP and CardiALLO programs have great promise as valuable therapeutics for the treatment of ischemic heart failure of reduced ejection fraction. We look forward to the presentations and discussions at the conference.”

About the CardiAMP Autologous Cell Therapy Program

CardiAMP Cell Therapy – FDA designated as a Breakthrough therapy – uses a patient’s own (autologous) bone marrow cells delivered to the heart in a minimally invasive, catheter-based procedure to potentially stimulate the body’s natural healing response. CardiAMP Cell Therapy incorporates three proprietary elements not previously utilized in investigational cardiac cell therapy: a pre-procedural cell analysis for patient selection, a high target dosage of cells, and a proprietary delivery system that has been shown to be safer than other intramyocardial delivery systems and exponentially more successful in cell retention. The CardiAMP HF trial is supported by the Maryland Stem Cell Research Fund and the Centers for Medicare and Medicaid Services. The proprietary CardiAMP cell procedure kits and their dedicated proprietary catheter delivery system are manufactured at BioCardia’s facility in Sunnyvale, California. CAUTION - Limited by United States law to investigational use.