Safety Board Recommends BioCardia's Heart Failure Cell Therapy To Continue Unchanged

The independent Data Safety Monitoring Board (DSMB) has completed its prespecified data review for BioCardia Inc's (NASDAQ:BCDA) ongoing Phase 3 CardiAMP Cell Therapy Heart Failure Trial.

  • The DSMB based its review on all available data for the 108 patients enrolled with an additional six crossover patient procedures in the trial to date. 
  • The monitoring board's assessment indicated no significant safety concerns and recommended that the study continue as designed.  
  • The ongoing CardiAMP Heart Failure Trial is expected to enroll 260 patients. 
  • CardiAMP Cell Therapy System received FDA Breakthrough Device status for heart failure earlier this month.
  • The trial's primary endpoint is an outcomes composite score based on a hierarchical analysis of the three-tiered Finkelstein-Schoenfeld (FS).
  • The FS procedure is a ranked analysis that compares the occurrence of cardiovascular and other health-related events, along with functional capacity measures, through one year in patients.
  • Price Action: BCDA shares are down 4.10% at $2.34 during the market session on the last check Monday.
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