COBRA PzF NanoCoated Coronary Stent
Commercial- Indications
- Coronary artery disease
Company intelligence / Profile preview
The COBRA PzF stent met pre-specified performance goals for both the primary endpoint of target vessel failure and the secondary endpoint of angiographic late lumen loss at 9-months post-intervention in the PzF SHIELD clinical trial[7]. The company also received FDA approval for an IDE clinical trial for Oncozene embolic microspheres loaded with doxorubicin for hepatocellular carcinoma treatment[6].
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