course of therapy and blood pressure should be
monitored weekly during the first six weeks of therapy and treated
as needed. Incidence of bleeding regardless of causality was 15%
for Nexavar vs. 8% for placebo and the incidence of
treatment-emergent cardiac ischemia/infarction was 2.9% for Nexavar
vs. 0.4% for placebo. Most common treatment-emergent adverse events
with Nexavar were diarrhea, rash/desquamation, fatigue, hand-foot
skin reaction, alopecia, and nausea. Grade 3/4 adverse events were
38% for Nexavar vs. 28% for placebo. Women of child-bearing
potential should be advised to avoid becoming pregnant and advised
against breast-feeding. In cases of any severe or persistent side
effects, temporary treatment interruption, dose modification or
permanent discontinuation should be considered.
For U.S. Nexavar prescribing information, visit www.nexavar.com or call
1.866.NEXAVAR (1.866.639.2827).
About Onyx Pharmaceuticals, Inc.
Onyx Pharmaceuticals, Inc. is a biopharmaceutical company
developing innovative therapies that target the molecular
mechanisms that cause cancer. The company is developing Nexavar(R),
a small molecule drug, with Bayer Pharmaceuticals Corporation.
Nexavar has been approved for the treatment of advanced kidney
cancer. For more information about Onyx's pipeline and activities,
visit the company's web site at: www.onyx-pharm.com.
About Bayer HealthCare
Bayer HealthCare Pharmaceuticals Inc. is the U.S.-based
pharmaceuticals unit of Bayer HealthCare LLC, a division of Bayer
AG. One of the world's leading, innovative companies in the
healthcare and medical products industry, Bayer HealthCare combines
the global activities of the Animal Health, Consumer Care, Diabetes
Care, and Pharmaceuticals divisions. In the United States, Bayer
HealthCare Pharmaceuticals comprises the following business units:
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Page: 1 2 3 4 5 6 7 Related medicine technology :1.
Review of Nexavar Data Presented at ASCO 2007- Investor Conference
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