Micromet and MedImmune are developing MT103 under the terms of a 2003 agreement in which MedImmune has obtained exclusive rights for the BiTE antibody in North America. Micromet has retained the rights to MT103 outside of North America.
About Micromet, Inc. (http://www.micromet-inc.com)
Micromet, Inc. is a biopharmaceutical company developing novel,
proprietary antibodies for the treatment of cancer, inflammation and
autoimmune diseases. Three of its antibodies are in clinical development.
MT103 (MEDI-538), the first antibody in Micromet's product pipeline
developed utilizing the BiTE(R) antibody technology platform, is being
evaluated in a phase 2 clinical trial for the treatment of patients with
acute lymphoblastic leukemia, and in a phase 1 clinical trial for the
treatment of patients with non-Hodgkin's lymphoma. BiTE antibodies
represent a new class of therapeutic antibodies that activate a patient's
own cytotoxic T cells to eliminate cancer cells. Micromet is developing
MT103 in collaboration with MedImmune, a subsidiary of Astra Zeneca plc.
The second clinical stage antibody is adecatumumab (MT201), a human
monoclonal antibody targeting EpCAM expressing tumors. Adecatumumab is
being developed by Micromet in collaboration with Merck Serono in a phase
1b clinical trial evaluating adecatumumab in combination with docetaxel for
the treatment of patients with metastatic breast cancer. The third clinical
stage antibody is MT293 (formerly D93), also known as TRC093, a
first-in-class humanized monoclonal antibody that inhibits angiogenesis and
tumor cell growth by binding cleaved collagen. MT293, which is currently
being tested in a phase 1 clinical trial, is licensed to TRACON
Pharmaceuticals, Inc. and is being developed for the treat
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