ompared with radiation therapy alone. The following sites were
affected: salivary glands (65%/56%), larynx (52%/36%), subcutaneous
tissue (49%/45%), mucous membranes (48%/39%), esophagus (44%/35%),
skin (42%/33%), brain (11%/9%), lung (11%/8%), spinal cord (4%/3%),
and bone (4%/5%) in the ERBITUX and radiation versus radiation
alone arms, respectively.
The incidence of Grade 3 or 4 late radiation toxicities were
generally similar between the radiation therapy alone and the
ERBITUX plus radiation therapy arms.
The most common adverse events seen in patients with carcinomas
of the head and neck receiving ERBITUX in combination with
radiation therapy (n=208) versus radiation alone (n=212) were
mucositis-stomatitis (93%/94%), acneform rash (87%/10%), radiation
dermatitis (86%/90%), weight loss (84%/72%), xerostomia (72%/71%),
dysphagia (65%/63%), asthenia (56%/49%), nausea (49%/37%),
constipation (35%/30%) and vomiting (29%/23%). The most common
adverse events seen in patients with carcinomas of the head and
neck receiving ERBITUX as a single agent (N=103) were acneform rash
(76%), asthenia (45%), pain (28%), fever (27%) and weight loss
(27%).
The most common adverse events seen in patients with mCRC
receiving ERBITUX with irinotecan (n=354) or ERBITUX as a single
agent (n=420) were acneform rash (88%/90%), asthenia/malaise
(73%/48%), diarrhea (72%/25%), nausea (55%/29%), abdominal pain
(45%/26%), vomiting (41%/25%), fever (34%/27%), constipation
(30%/26%), and headache (14%/26%).
ImClone Systems Incorporated is committed to advancing oncology
care by developing a portfolio of targeted biologic treatments
designed to address the medical needs of patients with a variety of
cancers. The Company's research and development programs include
growth factor blockers and angiogenesis inhibitors. ImClone
Systems' strategy is to become a fully integrated biopharmaceutical
company, taking its development programs from the research stage to
the market. Im
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Page: 1 2 3 4 5 6 7 8 9 Related medicine technology :1.
Data Available From Erbitux Phase III Study in First-Line Treatment
of Advanced Lung Cancer2.
Positive Results Prompt US National Cancer Institute to Make Glivec
Available to Patients in Post-Surgical GIST Study3.
Positive Results Prompt US National Cancer Institute to Make
Gleevec Available To Patients in Post-Surgical Gist Study4.
Survival Data Available From Erbitux Study in First-Line Treatment
of Advanced Head and Neck Cancer5.
Survival Data Available from Erbitux Study in First-Line Treatment
of Advanced Head and Neck Cancer6.
Extensive Clinical Data on Erbitux Presented at the 2007 ASCO
Annual Meeting7.
Merck at ASCO 2007: Spectrum of Studies Reinforces Promise of
Erbitux for Colorectal and Head and Neck Cancer Patients8.
Randomized Phase III Trial Showed Erbitux Significantly Improved
Secondary Endpoints of Progression-Free Survival and Disease
Control in Metastatic Colorectal Cancer Patients9.
Phase 3 Results for Dabigatran Etexilate, an Investigational Oral
Anticoagulant, Presented Today at the XXIst Congress of the
International Society on Thrombosis and Haemostasis10.
YM BioSciences Announces Secondary Efficacy and Safety Findings in
Randomized Phase IIB Aerolef Trial11.
Portola Pharmaceuticals Announces Positive Data from a Phase II
Study of its Factor Xa Inhibitor at the XXI Congress of the
International Society on Thrombosis and Haemostasis