Healthcare Industry News: alitretinoin
News Release - April 29, 2009
Basilea's Toctino(R) Receives Marketing Authorization in NetherlandsBASEL, SWITZERLAND--(Healthcare Sales & Marketing Network)--Apr 29, 2009 -- Basilea Pharmaceutica Ltd. (Swiss:BSLN.SW ) announces that ToctinoŽ (alitretinoin), a new once-daily oral treatment for adults with severe chronic hand eczema (CHE) unresponsive to potent topical corticosteroids, has been approved by the Dutch Medicines Evaluation Board (MEB).
Subsequent to the recommendation for regulatory approval under the European decentralized procedure, Basilea received the marketing authorization for ToctinoŽ in Netherlands. Following the regulatory approval of ToctinoŽ in Netherlands, Basilea will submit a pricing and reimbursement dossier to the country authorities.
Chronic hand eczema - a debilitating skin disease
Hand eczema is a common inflammatory skin disease and is often chronic and relapsing. Hand eczema is reported to affect up to ten percent of the general population. The more severe, chronic form of the condition is thought to affect five to seven percent of these patients, causing impaired use of their hands and a considerable impact on their ability to perform everyday activities.
ToctinoŽ (alitretinoin), the only therapy approved for severe chronic hand eczema unresponsive to potent topical corticosteroids
ToctinoŽ (alitretinoin) was developed by Basilea Pharmaceutica International Ltd.
The MEB approved ToctinoŽ for the use in adults who have severe CHE that is unresponsive to treatment with potent topical corticosteroids.
ToctinoŽ is a once-daily oral therapy for the treatment of adults that is given for 12 to 24 weeks, depending on patient response. In the six-month post-treatment observation in the pivotal phase III clinical trials, patients who responded to ToctinoŽ experienced long periods free from relapse and improved patient satisfaction.
ToctinoŽ has been launched in Denmark, Germany and the United Kingdom, and has also received marketing authorization in Austria, Belgium, Finland, France and Luxemburg. In addition, ToctinoŽ has been recommended for approval in two additional EU Member States and is under regulatory review in Switzerland, Canada and 15 additional European countries.
In the largest ever phase III clinical trial program in CHE, ToctinoŽ was the first treatment to show effective clearing of severe CHE, with clear or almost clear hands achieved in nearly 50 percent of patients treated 30 mg ToctinoŽ.
ToctinoŽ is a known teratogen (a substance that can cause birth defects when women are exposed during pregnancy). Strict pregnancy prevention one month before, during, and one month after cessation of treatment as well as monthly pregnancy testing are required for women of childbearing age. A comprehensive pregnancy prevention program for ToctinoŽ has been developed and implemented.
In clinical trials, ToctinoŽ was well tolerated and demonstrated a safety profile overall consistent with the retinoid class. Overall, the most frequently reported adverse events in the phase III clinical trials were headache and increased levels of blood lipids. Side effects were dose-dependent.
A phase III clinical trial on alitretinoin for the treatment of severe chronic hand eczema is ongoing in the U.S.
Basilea Pharmaceutica Ltd. is headquartered in Basel, Switzerland, and listed on the SIX Swiss Exchange (Swiss:BSLN.SW ). Basilea's integrated research and development operations are currently focused on new antibacterial, antifungal and oncology agents to fight drug resistance and on the development of dermatology drugs. Basilea's products are targeted to satisfy high medical and patient needs in the hospital and specialty care setting. The company owns a diversified portfolio including two commercialized drugs (alitretinoin, ceftobiprole) and one investigational drug in phase III (isavuconazole). ToctinoŽ (alitretinoin) is marketed in the United Kingdom, Denmark and Germany and is approved in Austria, Belgium, Finland, France, Luxemburg and Netherlands. alitretinoin has been recommended for approval in two additional EU Member States and is under regulatory review in Canada, Switzerland and 15 additional European countries. Furthermore a phase III clinical trial on alitretinoin for the treatment of severe chronic hand eczema is ongoing in the U.S. Ceftobiprole is marketed in Canada and Ukraine under the brand name ZEFTERA(TM) and in Switzerland under Zevtera(TM). Marketing applications for ceftobiprole were submitted in the U.S., the EU and several other countries. The company has set up commercial organizations in UK, Denmark, Germany and Canada, while it is building sales and marketing organizations in other countries to commercialize alitretinoin and to co-promote ceftobiprole, subject to approval.
This communication expressly or implicitly contains certain forward-looking statements concerning Basilea Pharmaceutica Ltd. and its business. Such statements involve certain known and unknown risks, uncertainties and other factors, which could cause the actual results, financial condition, performance or achievements of Basilea Pharmaceutica Ltd. to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. Basilea Pharmaceutica Ltd. is providing this communication as of this date and does not undertake to update any forward-looking statements contained herein as a result of new information, future events or otherwise.
This press release can be downloaded from www.basilea.com
Source: Basilea Pharmaceutica
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