CeloNova Announces Accelerated IDE Trial Enrollment Completion for Its COBRA PzF™ Coronary Stent System

SAN ANTONIO--()--CeloNova BioSciences, Inc. announced completion of patient enrollment in the global, multi-center IDE trial for its COBRA PzF stent. Completed enrollment was ahead of schedule and supports submission for FDA approval of the novel COBRA PzF stent with its advanced, nano-thin coating of Polyzene™-F polymer.

“We are excited to have completed this important milestone, with the involvement of outstanding study investigators under the leadership of Principal Investigator Professor Donald Cutlip, MD, of the Harvard Medical School in Boston, Massachusetts and Co-Principal Investigator Professor Sigmund Silber, MD, PhD of the University of Munich, Germany,” stated Martin Landon, CEO of CeloNova BioSciences. “Completion of enrollment ahead of schedule suggests that there is very high interest in the disruptive potential of our stent.”

“We wish to thank and congratulate the research teams in all participating centers for their hard work,” said Professor Cutlip. “We anxiously await the final study results and look forward to a stent that potentially meets an unmet need for patients who are unable or unwilling to be compliant with long term dual anti-platelet therapy (DAPT).”

“The Polyzene-F nano-coating may make the stent surface resistant to thrombus and may help reduce inflammation,” said CeloNova Chief Technology Officer Jane Ren. “Furthermore, the COBRA PzF stent's advanced thin strut design may help minimize vessel wall injury, and may enable a more rapid and natural healing. We look forward to generating the data that will allow us to bring to market a product that may significantly improve patient care, while reducing cost, across the full care continuum.”

About the Company

CeloNova BioSciences, Inc. is a global medical device company that develops, manufactures and markets a family of Interventional Cardiology and Endovascular products. For additional information about CeloNova BioSciences and this press release, see the company website at http://celonova.com/wp-content/uploads/PzFSHIELDComplete.pdf.

Contacts

for CeloNova BioSciences, Inc.
Jim Dublin, 210-227-0221
jdublin@dublinandassociates.com

Release Summary

CeloNova BioSciences announced completion of patient enrollment in global, multi-center IDE trial for its COBRA PzF stent. Enrollment supports submission for FDA approval of novel COBRA PzF stent.

Contacts

for CeloNova BioSciences, Inc.
Jim Dublin, 210-227-0221
jdublin@dublinandassociates.com