palonosetron intravenous / Generic mfg. 
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 72 Diseases   11 Trials   11 Trials   447 News 


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  • ||||||||||  cisplatin / Generic mfg.
    Trial initiation date:  Cisplatin Disposition and Kidney Injury (clinicaltrials.gov) -  Mar 22, 2019   
    P=N/A,  N=72, Not yet recruiting, 
    Palonosetron is non-inferior and cost-effective compared to ondansetron for prevention of acute chemotherapy-induced vomiting (CIV) in children receiving moderate and high emetogenic chemotherapy. Initiation date: Jan 2019 --> Apr 2019
  • ||||||||||  cisplatin / Generic mfg.
    New trial:  Cisplatin Disposition and Kidney Injury (clinicaltrials.gov) -  Jan 28, 2019   
    P=N/A,  N=72, Not yet recruiting, 
  • ||||||||||  oxaliplatin / Generic mfg., leucovorin calcium / Generic mfg., palonosetron intravenous / Generic mfg.
    Clinical, Journal:  A patient with oxaliplatin immune-induced syndrome (OIIS) who also developed leucovorin and palonosetron-associated thrombocytopenia. (Pubmed Central) -  Oct 21, 2018   
    To our knowledge, these two drugs have never been described in the literature as a cause of DDPA. We suggest that OIIS in addition to oxaliplatin-induced thrombocytopenia may be associated with the development of DDPAs to other drugs causing clinically significant thrombocytopenia which is important to recognize and manage with discontinuation of provoking agents.
  • ||||||||||  Varubi (rolapitant oral) / TerSera Therap, GSK, netupitant (Ro 67-3189) / Helsinn, Otsuka
    Review, Journal, CINV:  Recent Advances in Preventing Chemotherapy-Induced Nausea and Vomiting. (Pubmed Central) -  Jun 22, 2018   
    The US Food and Drug Administration has recently approved new therapies for prevention of CINV, including the neurokinin-1 (NK1) receptor antagonist rolapitant and the fixed-dose combination of the second-generation 5-hydroxytryptamine type 3 receptor antagonist palonosetron with the novel NK1 receptor antagonist netupitant...This article will address changes in CINV guidelines over the past 5 years and provide updates on recently approved agents and agents that are expected to be approved, based on published phase III trials. It will also explore other factors affecting optimal CINV control, including the role of patient-related risk factors and the role of physician adherence to antiemetic guidelines in reducing the residual risk of CINV.