Literature DB >> 31984777

Safety of antiemetic prophylaxis with HTX-019 as a 30-min infusion in patients with cancer: a retrospective study.

Toni S Perry1, Natalie Dickson2, Jeffrey F Patton2.   

Abstract

Aim: The NK-1 receptor antagonist HTX-019 (CINVANTI® [aprepitant injectable emulsion]) was approved for preventing chemotherapy-induced nausea and vomiting based on bioequivalence studies in healthy volunteers. The objective of this study was to evaluate HTX-019 safety in cancer patients. Patients & methods: This retrospective analysis evaluated the safety of HTX-019 130 mg 30-min intravenous infusion, as part of a three-drug antiemetic regimen.
Results: No treatment-emergent adverse events (TEAEs) were deemed related to HTX-019. During treatment cycles, three of 100 patients developed five reversible TEAEs: dyspnea, hot flash, pain, nausea and visual disturbance. Between cycles, six patients had TEAEs of dizziness (three patients), infusion-site events (two patients) and headache (two patients).
Conclusion: HTX-019 is safe in cancer patients receiving chemotherapy.

Entities:  

Keywords:  CINV; HTX-019; adverse events; aprepitant; intravenous infusion; retrospective; safety

Year:  2020        PMID: 31984777     DOI: 10.2217/fon-2019-0835

Source DB:  PubMed          Journal:  Future Oncol        ISSN: 1479-6694            Impact factor:   3.404


  1 in total

1.  Best Practice Approach to Successful Conversion of Fosaprepitant to Aprepitant IV in a Large Multisite Community Oncology Infusion Center: A Retrospective Analysis.

Authors:  Derek Burns; Julianna Kula; Scott Marshall; Elizabeth Ashworth; Matthew Ornelas
Journal:  Adv Ther       Date:  2020-05-23       Impact factor: 3.845

  1 in total

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