iVascular’s Luminor 18 drug-eluting balloon, has received CE mark approval.
Boston Scientific has announced that its GreenLight XPS laser therapy system, used for the treatment of prostatic enlargement, known as benign prostatic hyperplasia, received positive guidance from the National Institute for Health and Care Excellence (NICE).
Gore has received CE mark for its Excluder conformable abdominal aortic aneurysm (AAA) device, a product designed for the treatment of abdominal aortic aneurysms in patients with challenging anatomies.
Bayer has announced that a phase III trial evaluating its oncology compound Stivarga (regorafenib) tablets for the treatment of patients with unresectable hepatocellular carcinoma has met its primary endpoint of a statistically significant improvement in overall survival.
Scott Trerotola, Stanley Baum professor of Radiology and chief, Vascular and Interventional Radiology, University of Pennsylvania Medical Center, Philadelphia, USA, discussed how competition improves interventional radiology, while delivering the Dr Charles T Dotter Lecture at the 2016 Society of Interventional Radiology (SIR) annual meeting in Vancouver, Canada.
Many physicians now believe that immunotherapy is a disruptive field in cancer medicine. Interventional oncology can either “snooze and lose” as one prominent interventional radiologist put it on a recent podium presentation, or wake up and do the research needed on how best to harness the potential of this field when using interventional oncology treatments.
The Asia-Pacific Hepatocellular Carcinoma Trials Group (AHCC) protocol 06 SIRveNIB randomised controlled study of SIR-Spheres Y-90 resin microspheres versus sorafenib in the treatment of unresectable primary liver cancer (hepatocellular carcinoma or HCC) has completed its target enrolment of at least 360 patients.
The US Food and Drug Administration (FDA) has finalised its efforts to streamline the “compassionate use” process, used by physicians to access investigational drugs and biologics for patients with limited treatment options.
A new bill introduced to the US Senate by Senator Dan Coats seeks to address the gap between the US Food and Drug Administration (FDA)’s priority review process for breakthrough medical devices, and the Centers for Medical and Medicare Services’ (CMS) review system for reimbursement.
Sirtex has announced that Discovery Health, a South African private health insurer, has agreed to reimburse Sir-Spheres Y-90 resin microspheres for the treatment of all forms of inoperable liver tumours. Sir-Spheres Y-90 resin microspheres are a medical device used in an interventional radiology procedure known as SIRT or radioembolisation, which targets high doses of radiation directly to liver tumours.
Lombard Medical, has announced the 30-day clinical results from 57 patients that were implanted with the Altura endograft system. The 57 patients were implanted by Albrecht Krämer at the Pontificia Universidad Católica de Chile Hospital in Santiago, Chile, and Dainis Krievins, professor and department head of Vascular and Endovascular Surgery at the Pauls Stradins Clinical University Hospital in Riga, Latvia.
What if physicians could perform an optical biopsy (defined by Thomas D Wang, associate professor, Gastroenterology, University of Michigan, USA, as one that uses the properties of light to enable the operator to make an instant diagnosis at endoscopy)? Further, what if during a cryoablation procedure, an interventional radiologist can actually see what happens during the procedure at a cellular level in real time? A new tool, Cellvizio (Mauna Kea) does just that.
A study conducted at St Thomas’ Hospital, London, UK, indicates that the VeinCLEAR catheter (RF Medical) produces good results when used in radiofrequency ablation in the treatment of lower extremity superficial venous insufficiency. The study team, led by Adam M Gwozdz, now suggest that “Long-term evaluation of this device is now needed to ensure that these encouraging early results are maintained.”
Ethicon has announced a definitive agreement to acquire NeuWave Medical. Financial terms of the transaction have not been disclosed.
Auris Surgical Robotics and Hansen Medical today announced that they have signed a definitive merger agreement under which Auris will acquire Hansen Medical for US$4.00 per share in cash, or a total equity value of approximately US$80 million.
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