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

CompletedOBSERVATIONAL
Enrollment

207

Participants

Timeline

Start Date

October 3, 2018

Primary Completion Date

December 30, 2019

Study Completion Date

January 30, 2020

Conditions
Chemotherapy-Induced Nausea and Vomiting
Interventions
DRUG

300mg netupitant/0.5mg palonosetron hydrochloride

Antiemetic (NK1 receptor antagonist/5-HT3 receptor antagonist)

Trial Locations (17)

Unknown

Tom Baker Cancer Center, Calgary

The Moncton Hospital, Moncton

NSHA-QEII Health Sciences Centre, Halifax

Cape Breton Cancer Centre, Sydney

Royal Victoria Regional Health Centre, Barrie

William Osler Health System, Brampton

Grand River Regional Cancer Centre, Kitchener

London Health Sciences Centre, London

Thunder Bay Regional Health Sciences Centre, Thunder Bay

St. Michael's Hospital, Toronto

Sunnybrook Health Sciences Center, Toronto

Windsor Regional Cancer Centre, Windsor

Centre Integre de Sante et de Services Sociaux de la Monteregie-Centre, Greenfield Park

Cisss de Chaudiere-Appalaches, Lévis

Segal Cancer Centre-Jewish General Hospital, Montreal

Centre de recherche du CHUS and Hopital Fleurimont, Sherbrooke

Saskatoon Cancer Centre, Saskatoon

All Listed Sponsors
lead

Purdue Pharma, Canada

INDUSTRY

NCT03649230 - Observational Study on the Use of Akynzeo® in Patients Receiving HEC | Biotech Hunter | Biotech Hunter