Atlas Trials

A Study to Assess the Safety and the Efficacy of IV Fosnetupitant/Palonosetron (260 mg/0.25 mg) Combination Compared to Oral Netupitant/Palonosetron (300 mg/0.5 mg) Combination for the Prevention of CINV in AC Chemotherapy in Women With Breast Cancer

Clinical trial NCT03403712 · COMPLETED

Trial details

NCT number
NCT03403712
Sponsor
Helsinn Healthcare SA
Status
COMPLETED
Phase
Phase 3
Study type
INTERVENTIONAL
Chemotherapy-induced Nausea and Vomiting
Start date
2018-03-16
Primary completion
2018-09-19
Enrollment
404

View on ClinicalTrials.gov

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