Procyrion, Inc. announced the completion of a $57.7 million Series E funding round, including the conversion of $10.0 million of interim financing. The funds will be used to support the ongoing DRAIN-HF pivotal IDE trial evaluating the Aortix percutaneous mechanical circulatory support (pMCS) device in patients with acute decompensated heart failure (ADHF) who remain congested despite standard medical therapy (cardiorenal syndrome or CRS), as well as internal programs to improve product manufacturability and prepare for commercialization. The round was led by Fannin Partners in partnership with new and existing family/multi-family office investors.
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Company Information
Company
Procyrion
Location
3900 ESSEX LANE
Houston, Texas, United States
About
Procyrion™, Inc. is a privately held medical device company dedicated to providing effective treatment options for patients with cardiac and renal impairment. The company is developing the Aortix™ percutaneous mechanical circulatory support device, a catheter-deployed pump technology that uniquely harnesses fluid entrainment to pump blood to address multiple conditions with significant unmet needs. Aortix is limited by Federal law to investigational use only and is not approved for sale in any geography.
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