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October 2005 

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Hematological Cancer Therapeutics: 
Pipelines and Competition

Hermann A.M. Mucke, Ph.D.

New Page 1
Figure 1.1. B-Cell Cancers by Cell Development

Figure 1.2. Cancer Deaths by Gender, United States, 2004

Figure 1.3. The “Philadelphia Chromosome” Translocation

Figure 3.1. Prevention of Methylation-Induced Gene Silencing through Inhibition of DNA Methyltransferase Using Nucleoside Analogs

Figure 3.2. DNA Methyltransferase and Histone Deacetylase Enzymes Synergize to Prevent Access of Transcription Factors to DNA by Condensing Chromatin

Figure 4.1. The Chemical Structure of Thalidomide and Lenalidomide

Figure 4.2. Potential Antigen Targets for Immunotherapy in Leukemia

Figure 4.3. Activation and Proliferation of Patient T Cells by Autologous Chronic Lymphocytic Leukemia Cells before (Pre Rx) and 6 Months after (Post Rx) Infusion of Ad-CD154–Transduced CLL Cells

Table 1.1. Incidence and Annual Deaths from Main Types of Leukemias, United States, 2004

Table 3.1. FDA-Approved Monoclonal Antibody Drugs for Leukemia and Lymphomas

Table 3.2. Rituxan Adoption Rates in Non–Hodgkin’s Lymphoma and Chronic Lymphocytic Leukemia

Table 5.1. Drug Candidates with Submitted New Drug Applications or in Confirmed Active Phase III for Hematological Cancers

Table 5.2. New Chemical Entities in Top Clinical Stages I/II or II for Hematological Cancers

Table 5.3. Monoclonal Antibodies, Antisense Oligonucleotides, Cell Therapies, and Immunotoxins in Top Clinical Stages I, I/II, or II for Hematological Cancers
 


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