Yentreve (duloxetine hydrochloride) is now available in certain European countries, giving women suffering from moderate to severe stress urinary incontinence (SUI) a pharmaceutical treatment option for the first time.
Previous treatment options for SUI have been limited to conservative therapies and surgery. With the introduction of Yentreve, physicians in Germany, Denmark, Finland, Sweden and the United Kingdom now have a pharmaceutical treatment available that has been proven effective in significantly reducing the frequency of incontinence episodes and improving the quality of life of women with moderate to severe SUI. It is anticipated that Yentreve will launch in further European countries in the near future.
SUI, the most common form of urinary incontinence in women, affects one in seven women and is the accidental leakage of urine during physical activities such as sneezing, coughing, laughing, lifting or exercise. This distressing condition, affecting the social and emotional well-being of sufferers, leaves many women unable to enjoy daily activities such as exercising, laughing with friends or even lifting a child for fear of leakage. The majority of women with SUI do not seek professional help for their condition and are often too embarrassed to talk about it even with their closest friends.
"Yentreve is a perfect example of delivering on our commitment to provide first-in-class products. With Yentreve now available, women have even more reason to break their silence, talk to their physicians about this medical condition and ask for help," said Rich Pilnik, President of European Operations at Eli Lilly and Company.
Dr. Alessandro Banchi, Chairman of the Board of Managing Directors at Boehringer Ingelheim, added: "It is a milestone achievement to have Yentreve available in the markets for the first time. The relatively short time between approval and availability of Yentreve is testimony to the success of the partnership Boehringer Ingelheim has with Lilly and Boehringer Ingelheim's long standing expertise in urology. We look forward to making Yentreve available in many more countries in Europe in the coming months." The European Commission granted marketing authorization for Yentreve throughout the European Union for the treatment of moderate to severe stress urinary incontinence in women on August 12, 2004. The approval was based on ten studies across five continents involving more than 2,000 women with SUI. The studies demonstrated that Yentreve reduces the number of leakages by 50 to 100% in more than half of women with SUI, improves their quality of life and is generally well tolerated with mild and manageable side effects, the most common of which is transient nausea.
"Many women are reluctant to seek help from their doctors as they believe that little can be done to help them or that the only option is surgery. Hopefully Yentreve will bridge the gap that exists between pelvic floor exercises, which not all women can do or find helpful, and surgery, which is not appropriate or desirable for all women with stress urinary incontinence," said Linda Cardozo, Professor of Urogynecology, King's College Hospital, United Kingdom.
Simone, 47, an SUI sufferer from the United Kingdom, commented that "The condition was preventing me from exercising and leading my life to the full. It put me under great pressure to reconsider my career as a fitness instructor. Both physically and emotionally, life was becoming impossible. I had fantastic support from my husband, but not all women are as fortunate. A medicine gives the many women who aren't interested in surgery for SUI light at the end of the tunnel." Simone is the owner of two health clubs and a registered personal trainer and Pilates teacher.