NEW YORK--(BUSINESS WIRE)--Jun 5, 2007 - ERBITUX (cetuximab), the
first approved IgG1 monoclonal antibody targeting the epidermal
growth factor receptor (EGFR) developed and commercialized by
ImClone Systems Incorporated, was the focus of nine oral and 46
poster presentations at the recently concluded 43rd Annual Meeting
of the American Society of Clinical Oncology (ASCO).
This year's ASCO ERBITUX presentations showcased the extensive
clinical development of ERBITUX reporting Phase I through Phase III
clinical trial results in a broad range of cancers, including
colorectal, head and neck, non-small cell lung, pancreatic,
gastric, hepatocellular (liver), brain and ovarian cancer.
"We are very pleased with the extensive ERBITUX data that was
presented at ASCO. These findings should expand treatment options
for patients with cancer," said Alexander J. Denner, Ph.D.,
Chairman of ImClone System's Executive Committee. "The data
continue to validate the IgG1 monoclonal antibody platform upon
which the ImClone product pipeline is based."
Colorectal Cancer Highlights
Results from three Phase III studies (CRYSTAL, EPIC and NCIC
CO.17) discussed during oral presentations provide important
evidence of the clinical benefits demonstrated with ERBITUX
treatment across the continuum of care in metastatic colorectal
cancer. These three studies demonstrate significant improvements in
1st, 2nd and refractory mCRC patient outcomes including overall
survival, survival without disease progression, tumor shrinkage and
improvements in patient quality of life versus various standards of
care.
The Phase III CRYSTAL study, conducted by Merck KGaA, of ERBITUX
plus FOLFIRI (an irinotecan-based chemotherapy) in 1198 patients
with previously untreated metatstatic colorectal cancer (mCRC)
achieved its primary end point of improved survival without disease
progression - decreasing the risk of disease progression by
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