ncreased in patients receiving ERBITUX
alone or in combination with chemotherapy as compared to those
receiving best supportive care or chemotherapy alone based on
ongoing, controlled clinical trials in 244 patients. Approximately
one-half of these patients receiving ERBITUX experienced
hypomagnesemia and 10-15% experienced severe hypomagnesemia.
Electrolyte repletion was necessary in some patients and in severe
cases, intravenous replacement was required. Patients receiving
ERBITUX therapy should be periodically monitored for
hypomagnesemia, and accompanying hypocalcemia and hypokalemia
during, and up to 8 weeks following the completion of, ERBITUX
therapy.
The most serious adverse reactions associated with ERBITUX in
combination with radiation therapy in 208 patients with head and
neck cancer were infusion reaction (3%), cardiopulmonary arrest
(2%), dermatologic toxicity (2.5%), mucositis (6%), radiation
dermatitis (3%), confusion (2%), and diarrhea (2%).
The most serious adverse reactions associated with ERBITUX in
mCRC clinical trials (N=774) were infusion reaction (3%),
dermatologic toxicity (1%), interstitial lung disease (0.4%), fever
(5%), sepsis (3%), kidney failure (2%), pulmonary embolus (1%),
dehydration (5% in patients receiving ERBITUX with irinotecan, 2%
in patients receiving ERBITUX as a single agent) and diarrhea (6%
in patients receiving ERBITUX with irinotecan, 0.2% in patients
receiving ERBITUX as a single agent). The overall incidence of late
radiation toxicities (any grade) was higher with ERBITUX in
combination with radiation therapy compared 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 radia
'"/>
Page: 1 2 3 4 5 6 7 8 9 Related medicine technology :1.
Positive Results Prompt US National Cancer Institute to Make Glivec
Available to Patients in Post-Surgical GIST Study2.
Positive Results Prompt US National Cancer Institute to Make
Gleevec Available To Patients in Post-Surgical Gist Study3.
Data Available from Erbitux Phase III Study in First-Line Treatment
of Advanced Pancreatic Cancer4.
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