Respicardia Closes $58.5 Million In Financing To Treat Central Sleep Apnea

Company announces strategic relationship with ZOLL Medical

MINNETONKA, Minn., Dec. 18, 2017 /PRNewswire/ – Respicardia, Inc., a private medical technology company, announced today that the company has closed a $58.5 million financing, led by ZOLL Medical Corporation, a leading manufacturer of medical devices and related software solutions. All of Respicardia’s existing major investors helped to complete the financing round.

“We believe the remedē® System will soon become the treatment of choice for patients suffering from central sleep apnea and are pleased to receive significant funding from ZOLL in support of this important mission,” stated Bonnie Labosky, President and CEO of Respicardia. “Proceeds from the financing will be used to fund our U.S. commercialization efforts and support ongoing development of the system.”

Central Sleep Apnea (CSA) is a serious breathing disorder that disrupts the normal breathing pattern during sleep and negatively affects quality of life and overall cardiovascular health. CSA results from the brain’s inability to send appropriate signals to the respiratory muscles to stimulate breathing. The remedē System is clinically proven to safely and effectively treat moderate to severe CSA in adult patients and improve quality of life.

“The remedē System is a breakthrough technology that uniquely treats the devastating effects CSA has on a person’s quality of life and cardiovascular health,” explained Jonathan A. Rennert, CEO of ZOLL. “This investment in Respicardia exemplifies ZOLL’s commitment to advance novel therapies, especially those that address heart failure or one of its many co-morbidities such as central sleep apnea.”

The remedē System is a transvenous implantable neurostimulation system that stimulates the phrenic nerve, and engages the diaphragm to restore a normal breathing pattern during sleep in patients with CSA. The remedē System pivotal trial, published in The Lancet, demonstrated that transvenous neurostimulation with the remedē System can significantly reduce the severity of CSA, improve sleep, quality of life and patient satisfaction.

The remedē System received U.S. Food and Drug Administration (FDA) approval in October of 2017 and is commencing market release of the system in the United States.

About Respicardia

Respicardia is a private medical technology company dedicated to improving the lives of patients by developing implantable therapies designed to improve respiratory and cardiovascular health. The company’s initial product, the remedē System, is an implantable neurostimulation system designed to restore a more normal breathing pattern during sleep for moderate to severe central sleep apnea adult patients.

About ZOLL Medical Corporation

ZOLL Medical Corporation, an Asahi Kasei Group Company, develops and markets medical devices and software solutions that help advance emergency care and save lives, while increasing clinical and operational efficiencies. With products for defibrillation and monitoring, circulation and CPR feedback, data management, therapeutic temperature management, and ventilation, ZOLL provides a comprehensive set of technologies that help clinicians, EMS and fire professionals, and lay rescuers treat victims needing resuscitation and acute critical care. For more information, visit www.zoll.com.

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1 in 3 people with heart failure have Central Sleep Apnea and stop breathing during the night. Talk to your doctor about the remedē® System clinical study to see if you qualify.
Send us an email at info@respicardia.com or read about our clinical study at www.clinicaltrials.gov.

CONTACT US

Respicardia®, Inc.
12400 Whitewater Dr., Suite 150
Minnetonka, MN 55343 USA
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Phone: +1-952-540-4470
E-mail: info@respicardia.com
©2018 Respicardia®, Inc. The remedē® System has received FDA and CE Mark approvals. See Patents