- Einführung des Epoetin-alfa Biosimilar Binocrit® anfangs Dezember
- Binocrit® (Epoetin alfa) wird eingesetzt zur intravenösen Behandlung bei renaler Anämie und präoperativ bei der Eigenblutspende
- Binocrit® generiert 40% geringere Kosten als das Original
Sandoz - Pionier im Bereich Biosimilars - führt in diesen Tagen das Epoetin-alfa Biosimilar Binocrit® ein. Nachdem in der EU das Epoetin-alfa Biosimilar bereits 2007 eingeführt wurde, erhielt Sandoz in der Schweiz im Juli 2009 die Zulassung von der Nationalen Zulassungbehörde Swissmedic. Mit 40% Preisunterschied zum Original (gemessen an ex-factory Preisen) erlaubt Binocrit® ab sofort eine massgeblich kostengünstigere Behandlung der renalen Anämie.
Mit Sandoz Biosimilars die Zukunft sichern
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