See what 2 major guidelines have to say about palonosetron HCl       View in browser  
 
 
 
Full Prescribing Information       Physician Resources
 
Important Safety Information      Patient Resources
 
 
 
 
PREFERRED BY THE NATIONAL COMPREHENSIVE CANCER NETWORK (NCCN[R]) AND ASCO
Palonosetron: The preferred CINV therapy[1,2*]
 
DISCOVER WHY HCPs CHOOSE ALOXI
 
 
American Society of Clinical Oncology (ASCO).
 
* In adults receiving moderately emetogenic chemotherapy (MEC).  
 
 
  Indication  
  ALOXI® injection is indicated in adults for the prevention of acute and delayed nausea and vomiting associated with initial and repeat courses of moderately emetogenic chemotherapy, and the prevention of acute nausea and vomiting associated with initial and repeat courses of highly emetogenic chemotherapy.  
 
  Important Safety Information  
 
  CONTRAINDICATIONS  
 
 
ALOXI is contraindicated in patients known to have hypersensitivity to the drug or any of its components
 
 
  Please see below for additional Important Safety Information.  
 
  NCCN and ASCO guidelines prefer palonosetron HCl  
 
  Palonosetron HCl is the preferred 5-HT3 receptor antagonist (RA) prior to MEC.1,2*  
 
  Palonosetron HCl is also recommended as an option for antiemetic regimens that include NK1 RAs and/or dexamethasone.1,2  
 
 
The only FDA-approved IV 5-HT3 RA indicated to prevent acute and delayed CINV in adult patients3*
 
 
   
 
Double-blind, randomized, phase III noninferiority trial comparing single doses of ALOXI (n=189) with ondansetron (n=185) with a primary endpoint of complete response during the acute phase (Day 1) following MEC. ALOXI demonstrated significantly greater complete response in the acute phase (81.0% vs 68.6%, p=0.0085) and in the delayed phase (74.1% vs 55.1%, p<0.001). Clinical superiority over other 5-HT3 receptor antagonists has not been adequately demonstrated in the acute phase.3,4  
 
  Important Safety Information (continued)  
 
  WARNINGS AND PRECAUTIONS  
 
 
Hypersensitivity reactions, including anaphylaxis, have been reported with or without known hypersensitivity to other 5-HT3 receptor antagonists
 
Serotonin syndrome has been reported with 5-HT3 receptor antagonists alone, but particularly with the use of serotonergic drugs. Serotonin syndrome can be life threatening. Symptoms may include the following combination of signs and symptoms: mental status changes, autonomic instability, neuromuscular symptoms, seizures, and gastrointestinal symptoms. Patients should be monitored for the emergence of serotonin syndrome, and if symptoms occur, discontinue ALOXI and initiate supportive treatment. Patients should be informed of the increased risk of serotonin syndrome, especially if ALOXI is used concomitantly with other serotonergic drugs
 
 
  ADVERSE REACTIONS  
 
 
In adults, the most commonly reported adverse drug reactions include headache (9%) and constipation (5%)
 
 
  For more information about ALOXI, please see Full Prescribing Information.  
 
  References: 1. Hesketh PJ, Bohlke K, Lyman GH, et al. Antiemetics: American Society of Clinical Oncology Focused Guideline Update. J Clin Oncol. 2016;34:381-386. 2. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for Antiemesis V2.2016. © National Comprehensive Cancer Network, Inc. 2016. All rights reserved. Accessed November 11, 2016. To view the most recent and complete version of the guideline, go online to NCCN.org. NATIONAL COMPREHENSIVE CANCER NETWORK®, NCCN®, NCCN GUIDELINES®, and all other NCCN Content are trademarks owned by the National Comprehensive Cancer Network, Inc. 3. ALOXI® (palonosetron HCl) injection. Full Prescribing Information. 4. Gralla R, Lichinitser M, Van der Vegt S, et al. Palonosetron improves prevention of chemotherapy-induced nausea and vomiting following moderately emetogenic chemotherapy: results of a double-blind randomized phase III trial comparing single doses of palonosetron with ondansetron. Ann Oncol. 2003;14:1570-1577.  
 
 
 
ALOXI® is a registered trademark of Helsinn Healthcare SA, Switzerland, used under license. Distributed by Eisai Inc. under license of Helsinn Healthcare SA, Switzerland. Marketed by Eisai Inc. and Helsinn Therapeutics (U.S.), Inc.

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