Healthcare Industry News: alitretinoin
News Release - October 14, 2009
Basilea's Toctino(R) receives marketing authorization in SwitzerlandBASEL, SWITZERLAND, Oct., 14--(HSMN NewsFeed) - Basilea Pharmaceutica Ltd. announces that Toctino (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 Swiss regulatory authority Swissmedic.
"We are delighted that this innovative Basilea drug received marketing authorization in our home market. Toctino is the first licensed treatment for patients suffering from severe chronic hand eczema who do not respond to potent steroid therapy," said Dr. Anthony Man, CEO of Basilea. "We look forward to bring Toctino to patients and physicians in Switzerland soon."
Basilea submitted a pricing and reimbursement dossier to the Swiss authorities.
Toctino has been launched in Denmark, Germany and the United Kingdom for the treatment of adults with severe chronic hand eczema unresponsive to potent topical corticosteroids. Toctino has also received marketing authorization in Austria, Belgium, Finland, France, Luxemburg, the Netherlands and Spain. Further, Toctino has been recommended for approval in Italy. alitretinoin is under regulatory review in Canada and 15 additional European countries.
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 across Europe. It is characterized by thick, scaly skin that commonly gives rise to blisters, redness, swelling and painful cracks in the skin. 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.
Toctino (alitretinoin), the only therapy approved for severe chronic hand eczema unresponsive to potent topical treatments
Toctino was developed by Basilea Pharmaceutica International Ltd. Swissmedic approved Toctino for the use in adults who have severe refractory chronic hand eczema that is unresponsive to at least 4 weeks of extended topical treatment. The initial treatment includes the avoidance of contact to the causative irritant/noxa, skin protection and potent topical corticosteroids.
Toctino (alitretinoin) is a once-daily capsule to be taken with food. The recommended starting dose is 30 mg in most patients and a treatment course lasts up to 24 weeks depending on response.
alitretinoin is a naturally occurring, physiologic retinoid that is thought to work in CHE through anti-inflammatory and immunomodulatory effects.
alitretinoin 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 has been developed and implemented. In clinical trials alitretinoin was well tolerated and has a safety profile overall consistent with the retinoid class. Side effects were generally dose-dependent.
Basilea Pharmaceutica Ltd. is headquartered in Basel, Switzerland, and listed on the SIX Swiss Exchange (Swiss:BSLN ). 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 (Toctino, ZEFTERA(TM)/ Zevtera(TM)) and one investigational drug in phase III (isavuconazole). Toctino (alitretinoin) is marketed in the United Kingdom, Denmark and Germany and is approved in Austria, Belgium, Finland, France, Luxemburg, the Netherlands, Spain and Switzerland. alitretinoin has been recommended for approval in Italy and is under regulatory review in Canada 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 under the brand name ZEFTERA(TM) and in Switzerland under Zevtera(TM). Ceftobiprole is under regulatory review in the U.S., in 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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