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Fresenius Biotech obtains reimbursement approval for Removab® antibody in Belgium

04.10.2011

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Removab® receives approval for a shorter infusion time in treating malignant ascites – one-year survival rate in Removab®-treated patients is more than four times higher

20.09.2011

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Fresenius Biotech obtains reimbursement approval for Removab® antibody in Italy

22.06.2011

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ASCO 2011: Fresenius Biotech presents new data for the trifunctional antibody Removab® − benefit in overall survival of cancer patients demonstrated

07.06.2011

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Fresenius Biotech’s ATG-Fresenius S approved in Austria for GVHD prophylaxis in stem cell transplantations

06.06.2011

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Fresenius Biotech’s ATG-Fresenius S approved for GVHD prophylaxis in stem cell transplantations in Germany

07.03.2011

Fresenius Biotech is the first company in Germany to receive Paul-Ehrlich-Institut approval to use a polyclonal antibody in stem cell transplantations.

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Fresenius Biotech announces agreement with Swedish Orphan Biovitrum for distribution of Removab®

27.01.2011

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Removab® (Catumaxomab) wins Galenus-von-Pergamon award

21.10.2010

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Fresenius Biotech presents new data on trifunctional antibody Removab® at 46th ASCO Annual Meeting in Chicago

07.06.2010

The data show that overall survival significantly improved in patients who exhibit an early immune reaction subsequent to Removab®
treatment.

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Fresenius Biotech launches new corporate website

07.01.2010

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Removab® receives marketing approval

23.04.2009

European Commission grants marketing authorization for Removab®

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EMEA Committee recommends marketing approval

18.02.2009

The European Medicines Agency’s (EMEA) Committee for Medicinal Products for Human Use (CHMP) today issued a positive opinion recommending approval of Removab for the intraperitoneal treatment of malignant ascites.

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Removab Phase II Gastric

23.12.2008

Phase II study shows trifunctional antibody Removab® (catumaxomab) well tolerated in treatment of gastric cancer

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Removab Application for Marketing Authorization

21.12.2007

Fresenius Biotech applies for the marketing authorization of the trifunctional antibody Removab® for the treatment of malignant ascites

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Removab Phase II-III MA

17.07.2007

Secondary endpoints of phase II/III study confirm clear benefits from treatment with Removab® for patients with malignant ascites

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Removab Phase II-III

22.03.2007

Phase II/III pivotal study with trifunctional antibody Removab® shows encouraging results in malignant ascites from various cancers

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