Data presented today at the 8th European Congress on Menopause (EMAS) demonstrated that the majority of osteoporosis patients treated with EVISTA(R) (raloxifene) stay on therapy for the first two years.

300 postmenopausal osteoporosis patients received oral treatment with EVISTA(R). Patients were considered compliant if they had taken at least 80% of their medication.[1] Prof. Dr. P. Hadji, University Hospital of Giessen and Marburg GmbH, Marburg, Germany, said that "Results show that at 12, 24 and 36 months 96.4 %, 80.5% and 62% respectively of patients remained on therapy. The mean MPR was 52.8%. Finally 38.5% of all patients were classified adherent".

The treatment of osteoporosis among postmenopausal women represents a major public health challenge because long-term therapy is required to prevent fractures and chronic disability.[2] Today's results highlight the importance of good treatment compliance to help achieve therapeutic benefits for patients, and reduce the burden that osteoporosis places on individuals and the healthcare system.[3]

"Poor adherence has a negative effect on patient outcomes, and current treatment with many osteoporosis therapies tends to be suboptimal," commented Prof. Dr. P. Hadji, "However, EVISTA(R) has a long and proven history of patient compliance. Years of research not only confirm that patients adhere to treatment regimens with the drug, but also demonstrate a safety profile that is as strong now as it was when EVISTA(R) first came to market."

The data released today at EMAS comes in advance of EVISTA(R)'s 10th anniversary, a turning point that will not go unmarked. Coinciding with World Osteoporosis Day this October, plans are already underway to highlight EVISTA(R)'s continued success as a treatment for postmenopausal women with osteoporosis. Reinhard Bauer, DEO of DAIICHI SANKYO EUROPE, said "DAIICHI SANKYO is delighted to mark the 10th anniversary of EVISTA(R) later this year. The anniversary is intended to raise awareness of the disease and highlight the role that EVISTA(R) has played in transforming osteoporosis management over the years."

About EVISTA(R)

EVISTA(R) is a type of prescription medication called a Selective Estrogen Receptor Modulator (SERM). It is indicated for the treatment and prevention of osteoporosis in postmenopausal women. EVISTA(R) treats and prevents osteoporosis by reducing the risk of vertebral fractures.[4] EVISTA(R) has been taken by up to 26 million women worldwide, up to 7 million of them were treated in Europe.[5]

About DAIICHI SANKYO

DAIICHI SANKYO is a global pharmaceutical company that focuses on researching and marketing innovative medications. The company was created in 2005 through the merger of two traditional Japanese enterprises, Daiichi and Sankyo. With net sales of nearly 5.9 billion EUR in fiscal year 2008, DAIICHI SANKYO is one of the world's 20 leading pharmaceutical companies. The company's world headquarters is in Tokyo, and its European base is located in Munich. DAIICHI SANKYO has affiliates in 12 European countries and has been one of the strongest Japanese pharmaceutical companies located in Europe since it set up European production facilities and marketing offices in 1990. The company's research activities focus on the areas of cardiovascular diseases, hematology, diabetes, anti-infectives and cancer. Its aim is to develop medications that are "best" in their class or to create new classes of pharmaceutical drugs.

For more information, please visit: http://www.daiichi-sankyo.eu

References:

[1]. Hadji P, Wetzel K, Ziller V et al. (2009) Compliance during osteoporosis therapy with raloxifene. Poster presented at EMAS 2009

[2]. Turbi C, Herrero-Beaumont G, Acebes JC et al. (2004) Compliance and Satisfaction with Raloxifene Versus Alendronate for the Treatment of Postmenopausal Osteoporosis in Clinical Practice: An Open-Label, Prospective, Nonrandomized, Observational Study. Clin Therap 26; 245-256

[3]. Siris ES, Selby PL, Saag KG et al. (2009) Impact of Osteoporosis Treatment Adherence on Fracture Rates in North America and Europe. The American Journal of Medicine (2009) 122, S3-S13

[4]. Maricic M, Adachi JD, Sarkar S, Wu W, Wong M, Harper KD, (2002) Early effects of raloxifene on clinical vertebral fractures at 12 months in postmenopausal women with osteoporosis. Arch Intern Med.;162(10):1140-3.

[5]. Periodic safety Update Report, PSUR 16 Global (10-DEC-2007 TO 09-JUN 2008)/ Data on File

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DAIICHI SANKYO