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Observational Study on the Use of Akynzeo® in Patients Receiving HEC — EVOLVE_CINV  

Chemotherapy-Induced Nausea and Vomiting Clinical Trial

Official title:
A Phase IV, Real World Observational Study On The Use Of Akynzeo® (Netupitant/Palonosetron) For The Prevention Of Nausea and Vomiting in Oncology Patients Receiving Highly Emetogenic Chemotherapy (HEC) Over Multiple Cycles.

Clinical Trial Summary

This Canadian, multi-centre, prospective, observational real-world study is designed to collect patient-reported outcome data on the use of Akynzeo® (netupitant/palonosetron) for the prevention of nausea and vomiting in oncology patients receiving highly emetogenic chemotherapy (HEC).

Clinical Trial Description

The study will assess quality of life using the Functional Living Index of Emesis (FLIE) questionnaire and generate Real World Evidence in support of existing clinical trial data, including effectiveness and safety of Akynzeo® in the real world setting for the prevention of Chemotherapy Induced Nausea and Vomiting (CINV) in patients receiving highly emetogenic chemotherapy (HEC). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03649230
Study type Observational
Source Purdue Pharma, Canada
Contact
Status Completed
Phase
Start date October 3, 2018
Completion date January 30, 2020
View Details
See also
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