🇺🇸 FDA
Pipeline program

Bioequivalence study of the oral suspension of netupitant/palonosetron combination product versus the hard capsules of netupitant/palonosetron combination product after a single dose administration to healthy male and female volunteers in an open-label, randomised, single centre, 2-treatment, 4-period, 2 sequence replicative design

NEPA-23-01

Phase 1 other active

Quick answer

Bioequivalence study of the oral suspension of netupitant/palonosetron combination product versus the hard capsules of netupitant/palonosetron combination product after a single dose administration to healthy male and female volunteers in an open-label, randomised, single centre, 2-treatment, 4-period, 2 sequence replicative design for Healthy volunteers is a Phase 1 program (other) at Helsinn Birex Pharmaceuticals with 1 ClinicalTrials.gov record(s).

Program details

Company
Helsinn Birex Pharmaceuticals
Indication
Healthy volunteers
Phase
Phase 1
Modality
other
Status
active

Clinical trials