UNDERSTANDING AND ADDRESSING NEUROPATHY
ABRAXANE PHASE III MBC TRIAL


- The frequency and severity of sensory neuropathy increased with cumulative doses of ABRAXANE
- 3% of patients (7/229) discontinued treatment with ABRAXANE due to sensory neuropathy
- Only 1 incident of motor neuropathy (Grade 2) was observed in either arm of the controlled trial
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Additional Information for Readers Provided by Celgene Corporation
The clinical trial described in this article served as the
basis for the approval for ABRAXANE for Injectable Suspension.
The analyses contained in the article may differ from those in the package insert for ABRAXANE.
Please see Important Safety Information and Prescribing Information, including Boxed WARNING.
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Additional Information for Readers Provided by Bristol Myers Squibb
The clinical trial described in this article served as the
basis for the approval for ABRAXANE for Injectable Suspension.
The analyses contained in the article may differ from those in the package insert for ABRAXANE.
Please see Important Safety Information and Prescribing Information, including Boxed WARNING.
Click “OK” to proceed or “CANCEL” to return to
www.abraxanepro.com
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