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Celladon Corporation Announces Oral Presentation at American Heart Association of Long Term Follow-Up Results from the MYDICAR CUPID 1 Trial in Advanced Heart Failure
Date:11/18/2013

SAN DIEGO, Nov. 18, 2013 /PRNewswire/ -- Celladon Corporation, a clinical-stage biotechnology company focused on developing novel therapies by applying its leadership position in the field of SERCA enzymes, today announced that on behalf of the CUPID 1 Trial investigators, Dr. Barry H. Greenberg will present the full three year long-term follow up results from Phase 2a of the CUPID 1 trial in an oral presentation at the American Heart Association Scientific Sessions 2013 Conference held in Dallas, Texas. Phase 2a of the CUPID 1 trial investigated Celladon's product candidate MYDICAR in three dose groups for the treatment of advanced heart failure.

The details of the presentation are as follows:

  • Session Type: Abstract Oral Session
  • Session Title: 502. Novel Cell, Tissue Engineering, and Gene Based Strategies For Heart Failure
  • Abstract Title: Long Term Follow-up Of Patients With Advanced Heart Failure Following A Single Intracoronary Infusion Of AAV1/SERCA2a
  • Presentation Date/Time: 11/19/2013 9:00:00 AM Central time
  • Presenter: Barry H. Greenberg M.D., FACC, Director, Advanced Heart Failure Treatment Program; Professor of Medicine, University of California, San Diego

Dr. Greenberg stated, "The results of the long-term follow up of the CUPID patients at 36 months are a major step forward in the development of a promising new therapy for treating heart failure. Evidence of continued reduction in events with high dose MYDICAR compared to placebo extending out to 36 months and the persistence of transgene expression in the heart are very encouraging findings that support the possibility that MYDICAR has an important impact on the clinical course of heart failure patients."

"The durability of treatment effect and lack of safety concerns ob
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SOURCE Celladon Corporation
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