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FDA Grants CytoDyn Fast Track Designation for Leronlimab (PRO 140) in metastatic Triple-Ne

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A new algorithm takes cues from panoramic photography to merge massive, diverse cell datasets into a single source that

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Amgen Takes Sensipar Dispute to Appellate Court

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GlaxoSmithKline Slammed With $90 Million Verdict for Patent Infringement

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&#nl

Iliofemoral venous obstructive disease occurs when the flow of blood through the veins located deep in the pelvic region becomes blocked by a blood clot or compressed by anatomical anomalies. Endovascular treatment for venous obstructive disease is focused on restoring the normal flow of blood from the legs back to the heart. Because the iliofemoral veins are located deep in the pelvis, they may be subject to significant crushing forces from other anatomical structures such as the right common iliac artery. To help solve for this, the Vici stent system was designed to be uniformly strong and crush resistant, capable of restoring blood blow by creating a cylindrical, patent vessel.

&#nl

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According to Mahmood Razavi, MD, at Orange, CA-based St. Joseph Hospital, venous obstructive disease can cause quality of life issues without optimized treatment options.

&#nl

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&#nl

Boston Scientific noted that venous obstructive disease affects nearly 40% of the U.S. population and can be caused by conditions such as deep vein thrombosis, post-thrombotic syndrome, and compressive diseases such as May-Thurner syndrome. In patients with venous obstructions, blood may pool in the legs, resulting in pain, swelling, and skin ulcers.

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Boston Scientific has won FDA approval for its Vici Venous Stent System for the treatment of iliofemoral venous obstructive disease.

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&#nl

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&#nl

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Boston Scientific Launches New Stent for Venous Obstructive Disease

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Irvine, CA-based Endologix acquired the Ovation platform through its merger with TriVascular in February 2016. It's a low-profile device that has broadened the company's portfolio in terms of patients that can be treated. In June 2017, Endologix reported positive 30-day results from a study evaluating EVAR in women using the Ovation system.

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"His reasons for not using it more frequently were that there were limited data available and he believed it to be a technically challenging product to deploy," Onopchenko said. "And frankly, he chose as those initial cases, really a challenging reverse-tapered-neck presentation."

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Onopchenko said being able to purposefully explain to physicians "the why" behind each step in the process of deploying the endograft goes a long way toward changing how the Ovation device is perceived.

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3. Appreciation for Endologix in the EVAR Space

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Here are the reasons the physician gave Endologix for why he has begun to integrate Ovation into his practice since the facility visit.

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3. Appreciation for Endologix in the EVAR Space

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