Company intelligence / Profile preview

Endospan

Herzliya, Israelendospan.com ↗
Ownership
Private
Employees
~54
Development stage
Commercial
01

Overview

Endospan’s NEXUS system is the first and only approved branched endovascular stent graft for treating complex aortic arch disease, including aneurysms and dissections. The TRIOMPHE pivotal IDE trial has shown promising early results, with 30-day data demonstrating significant reduction in major adverse events compared to reference performance goals. The device is already approved and commercialized in Europe; U.S. approval is anticipated following completion of ongoing pivotal studies.

Therapeutic areas
Cardiovascular
Modalities
DeviceStent graft systemBiologic (as a device incorporating biologically compatible materials)
Industry
Implantable Medical Devices
02

Drug pipeline

2 assets

NEXUS

Commercial
Indications
Aortic arch aneurysm, Aortic arch dissection

1 more asset in the full pipeline.

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03

Partnerships

Artivion (strategic/financial partnership for U.S. FDA approval path)

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