Codman Neuro acquires Neuravi

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EmboTrap II

Codman Neuro has announced the acquisition of Neuravi. This acquisition comes after the company’s recent acquisition of Pulsar Vascular, expanding its products for stroke therapy. DePuy Ireland Unlimited Company, an affiliate of Codman Neuro, is the acquiring entity. Financial terms of the transaction were not disclosed.

Founded in 2009, Neuravi has invested extensively in scientific research on the varieties of clots that cause acute ischaemic stroke, and has translated learnings into its EmboTrap Revascularisation Platform. The EmboTrap device is engineered to restore blood flow to the brain by retrieving a clot with its proprietary dual-layer stent-like structure, and it has already been used to treat over 3,000 patients in Europe.

Globally, stroke is the second leading cause of death after the age of 60, and ischaemic strokes, caused by blockages in vessels supplying blood to the brain, account for 87% of all strokes. According to the European Journal of Neurology, the number of stroke events in Europe is projected to rise from 1.1 million in 2000 to 1.5 million per year by 2025, while the American Heart Foundation estimates someone dies of a stroke every four minutes. In the USA alone, the economic burden of stroke is estimated at US$33 billion annually, including the cost of health care services, medications, and lost productivity.

“Rapid restoration of flow is of utmost importance when treating stroke patients,” says Shlomi Nachman, Company Group Chairman of Johnson & Johnson Medical Devices Cardiovascular & Specialty Solutions. “The EmboTrap platform was designed to address this critical need and we are excited to combine Neuravi’s expertise in clot research with Codman Neuro’s global resources to accelerate innovation in acute ischaemic stroke treatment.”

The EmboTrap and EmboTrap II Revascularisation Devices are commercially available in Europe and have been available in the USA for investigational use only under the ARISE II clinical trial, which will support a US Food and Drug Administration (FDA) submission planned for later this year.