Radiance
Irvine, California firm receives a CE Mark for its RDX radioactive balloon brachytherapy device for treatment of de novo and restenotic coronary lesions. The RDX will be marketed to a few key customers, and then, following a formal launch at the Congress of the Society of Cardiology in Stockholm, Sweden Sept. 1-5, 2001, a widespread launch will start this fall. Meanwhile, Radiance expects to complete enrollment in the 480-patient BRITE II pivotal U.S. trial of the RDX by January 2002. Last January, Radiance began BRITE-SVG, a worldwide 50-patient Phase I trial of the RDX in saphenous vein grafts and in May began enrolling patients in RAPID, the European trial of the RDX in peripheral vessels. The company expects an IDE for a U.S. peripheral trial in the next few months
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Medtronic announced it received expanded MRI labeling for its DBS systems, which is critical, given that almost 70% of all DBS-eligible patients will likely need an MRI at some point in their care, says Ashwini Sharan, CMO for Medtronic Neuromodulation.
In this episode, Medtech Insight reporter Natasha Barrow speaks to LungLife AI CEO Paul Pagano. Lung Life AI is a US-based AIM-listed medical technology company that has developed a liquid biopsy test for the early detection of lung cancer called Lung LB. Pagano runs through the highlights of Lung Life AI journey to date and its future ambition for a strategic partnership. He also provides advice to similar diagnostic companies seeking reimbursement andcompliance with the US FDA Lab Developed Test ruling.
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