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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT01339260

Public ClinicalTrials.gov record NCT01339260. 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 Oct 25, 2026, 10:16 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, Double-dummy, Active-controlled, Parallel Group Study of the Efficacy and Safety of Oral Netupitant Administered in Combination With Palonosetron and Dexamethasone Compared to Oral Palonosetron and Dexamethasone for the Prevention of Nausea and Vomiting in Cancer Patients Receiving Moderately Emetogenic Chemotherapy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

NETU-08-18 is a two-arm clinical study assessing efficacy and safety of a single oral dose of netupitant and palonosetron, two antiemetic drugs, versus oral palonosetron, both given with oral dexamethasone. The objective of the study is to demonstrate that netupitant and palonosetron are more effective than palonosetron alone, to prevent nausea and vomiting induced by moderately emetogenic cancer chemotherapy after administration of repeated cycles of chemotherapy.

Study identification

NCT ID
NCT01339260
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Helsinn Healthcare SA
Industry
Enrollment
1,455 participants

Conditions and interventions

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
Apr 2011 (Type not available)
Primary completion
Nov 2012 (Actual)
Completion
Not listed
Last update posted
Nov 26, 2014

Started 2011

United States locations

U.S. sites
28
U.S. states
16
U.S. cities
27
Facility City State ZIP Site status
Anniston Oncology/Regional Medical Center Anniston Alabama 36207 —
Northwest Alabama Cancer Center Muscle Shoals Alabama 35661 —
Genesis Cancer Centre Hot Springs Arkansas 71913 —
Compassionate Cancer Care Medical Group Inc Corona California 92879 —
Compassionate Cancer Centre Medical Group Fountain Valley California 92708 —
American Institute of Research Los Angeles California 90017 —
Facey Medical Group Mission Hills California 91345 —
Compassionate Cancer Care Medical Group Riverside California 92501 —
American Institute of Research Whittier California 90603 —
Denver Health and Hospital Authority Denver Colorado 80204 —
Palm Beach Institute of Hematology and Oncology Boynton Beach Florida 33435 —
Baptist Cancer Institute Jacksonville Florida 32207 —
Deaconess Clinic Downtown Evansville Indiana 47713 —
Floyd Memorial Cancer Center of Indiana New Albany Indiana 47150 —
Kentucky Cancer Clinic Hazard Kentucky 41701 —
The John R Marsh Cancer Center Hagerstown Maryland 21742 —
Fallon Clinic at Worcester Medical Center Worcester Massachusetts 01608 —
Duke University Medical Center Durham North Carolina 27710 —
Piedmont Hematology Oncology Associates PA Winston-Salem North Carolina 27103 —
Tri-County Hematology and Oncolgy Associates Inc. Massillon Ohio 44646 —
Signal Point Clinical Research Center LLC Middletown Ohio 45042 —
Charleston Cancer Center Charleston South Carolina 29406 —
Charleston Hematology Oncology Charleston South Carolina 29414 —
Wellmont Medical Associates-Oncology and Hematology Bristol Tennessee 37620 —
Cancer Specialists of South Texas, P.A. Corpus Christi Texas 78412 —
The University of Texas Health Center Tyler Texas 75708 —
Northern Utah Associates Hematology / Oncology Ogden Utah 84403 —
Northwest Medical Specialties Tacoma Washington 98405 —

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 144 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01339260, 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 26, 2014 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01339260 live on ClinicalTrials.gov.

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