1. Current Status, Position:

Chairman of the Dept. of Hematology, Oncology, and Tumor Immunology at the HELIOS Clinic Berlin-Buch/Chairman of the DCGMA.

2. Education:

• 1979-1981: Dept. of Experimental Pharmacology at the Free University of Berlin, FRG
• 1982: Ph.D. degree in Medicine, Free University of Berlin, FRG
• 1981-1988: Clinical resident in the Dept. of Hematology and Oncology, University Clinic Steglitz, Free University of Berlin, FRG
• 1988: Degree for specialisation in Internal Medicine
• 1989: Degree for specialisation in Transfusion Medicine
• 1990: Habilitation for Internal Medicine, Free University of Berlin, FRG
• 1992: Degree for specialisation in Hematology and Oncology
• December 1993-March 2001: Deputy Medical Director, Dept. of Medical Oncology and Applied Molecular Biology (renamed 1996: Dept. of Hematology, Oncology, and Tumor Immunology), Robert Rössle Clinic, Charité, Campus Berlin-Buch, FRG
• Since 1994: Full Professor of Hematology/Oncology and Applied Molecular Biology with unlimited tenure, Humboldt University of Berlin
• Since April 2001: Medical Director and Head of the Dept. of Hematology, Oncology, and Tumor Immunology, Robert Rössle Clinic, HELIOS Klinikum Berlin-Buch, Charité, Campus Berlin-Buch, FRG
• 1994: Founding member of the "European Group for the Immunological Characterization of Leukemias" (EGIL)
• Since December 1999: in the board of the Drug Commission of the German Medical Association (DCGMA)
• 2002-2005: Full member and chairman of the Panel of Experts at the German Ministry of Health dealing with off label use of drugs
• Since 2004: Expert for risk management at the European Medicines Agency (EMEA); member of the Scientific Advisory Group (SAG)-Oncology
• Since 2006: Chairman of the Drug Commission of the German Medical Association (DCGMA)

3. Research Area:

Prof. Dr. Ludwig focuses his work on the following research areas:

• Biologic determinants of treatment response in acute leukemias (e.g., expression and function of apoptosis-related regulatory molecules, minimal residual disease); functional genomics both in translational research and model systems of acute leukemia (coordinator of the Acute Leukemia Consortium within the NGFN, National Genome Research Net);
• Innovative treatment strategies in oncology (e.g., bispecific monoclonal antibodies, targeted therapy);
• Pharmacovigilance, especially postmarketing surveillance; international harmonization of drug regulation/approvals;
• Issues of medical ethics and professional norms regarding academic-industry collaboration.