Noticias

Noticias

  • Título: FDA Approves BTG’s Varithena for Treatment of Varicose Veins
  • Fecha: 26-11-2013

  • London, UK, 26 November 2013: BTG plc (LSE: BTG), the specialist healthcare company, today announces that the US Food and Drug Administration (FDA) has approved Varithena™ (polidocanol injectable foam) for the treatment of patients with incompetent veins and visible varicosities of the great saphenous vein (GSV) system.1

    Varithena™ (formerly known as Varisolve® PEM) is a pharmaceutical-grade, low-nitrogen, polidocanol foam dispensed from a proprietary canister device. In two pivotal, placebo-controlled Phase III trials, VANISH-1 and VANISH-2, Varithena™ achieved a clinically meaningful improvement in the symptoms of superficial venous incompetence and the appearance of visible varicosities and addressed the underlying venous incompetence in the majority of patients treated.

    More than 30 million adults in the US aged 18 to 70 have varicose veins, with women twice as likely as men to develop varicosities. Varicose veins often require treatment for symptoms including leg pain, aching, heaviness, restless legs, cramps, throbbing, fatigue, itchiness, tingling and oedema. These symptoms are frequently the cause of absenteeism from work, disability and decreased quality of life.2

    Current treatments for varicose veins include thermal ablation and surgery. Varithena™ provides US physicians with the only approved comprehensive therapy to improve symptoms and appearance for a wide range of varicose veins, including incompetent GSV, accessory saphenous veins and visible varicosities of the GSV system both above and below the knee. Treatment is a minimally invasive, non-surgical procedure that requires neither tumescent anesthesia nor sedation.

    Louise Makin, CEO at BTG, said: “We are delighted to receive US approval for Varithena™, which we believe sets a new standard for the treatment of both the symptoms and appearance of varicose veins. We look forward to the commercial US launch in the second quarter of 2014, and to continuing to advance our plans to expand use into other geographies and into non-symptomatic veins.”



  • Fuente: endovascular.es