ment of non-Hodgkin's lymphoma (NHL), and various other hematologic
malignancies, solid tumors, and immunological disorders, pixantrone is
being developed by CTI to improve the activity and safety in treating
cancers usually treated with the anthracycline family of anti-cancer
agents. Anthracyclines have been shown to be very active clinically in a
number of tumor types, such as lymphoma, leukemia, and breast cancer. For
these diseases, anthracycline-containing chemotherapy regimens are
effective in first-line (initial) treatment. However, they may cause
cumulative heart damage that limits lifetime dosage and does not allow for
retreatment. Pixantrone has been designed to reduce the potential for heart
damage compared to currently available anthracyclines or anthracenediones
without a loss in anti-tumor or immunomodulatory activities.
About Brostallicin
Brostallicin, a novel synthetic second-generation DNA minor groove
binder, has potent cancer killing activity and has demonstrated synergism
in combination with standard cytotoxic agents as well as with newer
targeted therapies in preclinical experimental tumor models. Brostallicin
binds covalently to DNA within the DNA minor groove, interfering with DNA
division and leading to tumor cell death. More than 200 patients have been
treated with brostallicin in single-agent and combination studies.
Brostallicin had predictable and predominantly hematologic toxicities.
Activity was demonstrated in a number of solid tumor types. A phase II
study of brostallicin in relapsed/refractory soft tissue sarcoma met its
pre-defined activity and safety hurdles and resulted in a first-line phase
II study that is currently being conducted by the European Organization for
Research and Treatment of Cancer (EORTC).
About Non-Hodgkin's Lymphoma
Non-Hodgkin's lymphoma (NHL) is caused by the abnormal proliferation of
white blood cells and normally spreads through the lymphatic system, a
system of vessels that drai
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SOURCE Cell Therapeutics, Inc. Copyright©2008 PR Newswire. All rights reserved | |
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