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Completed Phase 3 Interventional Results available

A Safety Study of Oral Netupitant and Palonosetron for the Prevention of Nausea and Vomiting

ClinicalTrials.gov ID: NCT01376297

Public ClinicalTrials.gov record NCT01376297. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 6, 2026, 8:09 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III, Multicenter, Randomized, Double-blind, Unbalanced (3:1) Active Control Study to Assess the Safety and Describe the Efficacy of Netupitant and Palonosetron for the Prevention of Chemotherapy-induced Nausea and Vomiting in Repeated Chemotherapy Cycles.

Study identification

NCT ID
NCT01376297
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Helsinn Healthcare SA
Industry
Enrollment
413 participants

Conditions and interventions

Interventions

  • Aprepitant Drug
  • Dexamethasone Drug
  • Netupitant and Palonosetron Drug
  • Palonosetron Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2011
Primary completion
Aug 31, 2012
Completion
Not listed
Last update posted
Nov 16, 2014

Started 2011

United States locations

U.S. sites
11
U.S. states
8
U.S. cities
11
Facility City State ZIP Site status
Northwest Alabama Cancer Center PC Muscle Shoals Alabama 35661
East Valley Hematology and Oncology Medical Group Burbank California 91505
American Institute of Research Los Angeles California 90017
Veterans Administration New Jersey Health Care System East Orange New Jersey 07018
Hematology Oncology Associates of Rockland Nyack New York 10960
Hematology and Oncology Associates, Inc. Canton Ohio 44708
Tri-County Hematology & Oncology Associates, Inc Massillon Ohio 44646
Cancer Center at Memorial Hospital of RI Pawtucket Rhode Island 02860
Spartanburg Regional Health Services Spartanburg South Carolina 29303
South Texas Comrehensive Cancer Centers Corpus Christi Texas 78405
MD Anderson Cancer Center Houston Texas 77030-4009

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 64 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01376297, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 16, 2014 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01376297 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →