CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 43 enrolled
Drug / intervention
Netupitant +2 moredrug
Likely dose
Netupitant 300 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03097588
NCT03097588Phase 2Completed

A Phase II Clinical Trial of NEPA (Netupitant/Palonosetron) for Prevention of Chemotherapy Induced Nausea and Vomiting (CINV) in Patient Receiving the BEAM Conditioning Regimen Prior to Hematopoietic Cell Transplantation (HSCT)

OHSU Knight Cancer Institute·interventional·Posted Mar 31, 2017·Updated Jul 12, 2021

In Brief

A Phase 2 clinical trial evaluating Netupitant, Palonosetron Hydrochloride, and 1 other intervention for Malignant Neoplasm. Completed, enrolled 43 participants across 1 site.

Detailed Summary

This phase II trial studies how well netupitant and palonosetron hydrochloride work in preventing chemotherapy induced nausea and vomiting in patients with cancer undergoing BEAM conditioning regimen before stem cell transplant. Chemotherapy, such as carmustine, cytarabine, etoposide, and melphalan (BEAM), makes people feel sick to their stomach and causes vomiting. Netupitant and palonosetron hydrochloride may reduce the nausea and vomiting caused by the BEAM treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedMar 31, 2017
Enrollment StartApr 27, 2017
Primary CompletionFeb 20, 2020
Study CompletionMar 20, 2020
TodayJul 2, 2026
Enrollment to primary: 2.8 yearsPosted 9.3 years ago

Interventions

Netupitantdrug

300 mg, Given PO, QD

Palonosetron Hydrochloridedrug

0.5 mg, Given PO, QD

Questionnaire Administrationother

Ancillary studies