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SEMINAR ANNOUNCEMENT
Development of Immunotoxins for Targeted Cancer
Therapy
by
Koji Kawakami, M.D., Ph.D.
Department of Advanced Clinical Science and Therapeutics
Graduate School of Medicine
University of Tokyo
Tokyo, Japan
on
| Date: |
Friday, 25th November 2005 |
| Time: |
11.00 am to 12.00 noon |
| Venue: |
Seminar Room (S4-05-16)
Department of Pharmacy |
Abstract:
The progress of bioinformatics approach to understand
the characterization of cell-surface antigens or receptors on tumor
cells has stimulated the challenges to generate novel cancer vaccines
or neutralizing monoclonal antibody therapeutics. Among the targeted
cancer therapeutics, biologicals with targetable antibodies or ligands
conjugated or fused to toxins or chemicals for direct cell-killing
ability have been developed over the last two decades. These conjugated
or fused chimeric proteins are termed immunotoxins or cytotoxins.
Two targeted cytotoxins, DAB389IL-2 (ONTAKTM) targeting interleukin-2
receptors and CD33-calicheamycin (MylotargTM), have been approved
by the FDA for cutaneous T-cell lymphoma (CTCL) and relapsed acute
myeloid leukemia (AML), respectively. Immunotoxins including IL13-PE38QQR
are being tested in the Phase III clinical trial in the United States.
Immunoliposome is a liposome containing therapeutically active molecule
that is conjugated to ligand or antibody on the liposomal surface
to allow specific binding to the target cells. To develop new immunoliposomal
targeted drugs, we are currently in the process of establishing
a new laboratory in Biopolis, Singapore in collaboration with Oxygenix,
Co., Japan.
ALL ARE WELCOME
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