CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 171 enrolled / 171 target
Drug / intervention
Pazopanib Hydrochloride +9 moredrug
Likely dose
Not stated in 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/NCT01841736
NCT01841736Phase 2ActiveUpdate Overdue (1.1/mo)Completion was 87mo ago

Prospective Randomized Phase II Trial of Pazopanib (NSC #737754) Versus Placebo in Patients With Progressive Carcinoid Tumors

National Cancer Institute (NCI)·interventional·Posted Apr 26, 2013·Updated Jun 15, 2026

In Brief

A Phase 2 clinical trial evaluating Biospecimen Collection, Computed Tomography, and 8 other interventions for Foregut Neuroendocrine Tumor and 7 related conditions. Active but no longer recruiting, targeting 171 participants across 423 sites in 2 countries.

Signals

Enrollment appears stalled

Detailed Summary

This randomized phase II trial studies how well pazopanib hydrochloride works in treating patients with carcinoid tumors that are growing, spreading, or getting worse. Pazopanib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Study Details

Timeline

Phase 2Active
201320142015201620172018201920202021202220232024202520262027
First PostedApr 26, 2013
Enrollment StartSep 20, 2013
Primary CompletionMar 5, 2019
Study CompletionSep 10, 2026
TodayJul 2, 2026
Enrollment to primary: 5.5 yearsPosted 13.2 years ago

Arms & Interventions

Arm I (pazopanib hydrochloride)experimental

Patients receive pazopanib hydrochloride PO QD on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo ECHO or MUGA during screening. Patients also undergo CT, MRI, and chest x-ray throughout the trial. Patients may optionally undergo blood sample collection during screening and on study.

Procedure: Biospecimen CollectionProcedure: Computed TomographyProcedure: Echocardiography TestOther: Laboratory Biomarker AnalysisProcedure: Magnetic Resonance ImagingProcedure: Multigated Acquisition ScanDrug: Pazopanib HydrochlorideOther: Quality-of-Life AssessmentProcedure: X-Ray Imaging
Arm II (placebo)placebo_comparator

Patients receive placebo PO QD on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. At the time of progressive disease, patients may cross-over to Arm I. Patients undergo ECHO or MUGA during screening. Patients also undergo CT, MRI, and chest x-ray throughout the trial. Patients may optionally undergo blood sample collection during screening and on study.

Procedure: Biospecimen CollectionProcedure: Computed TomographyProcedure: Echocardiography TestOther: Laboratory Biomarker AnalysisProcedure: Magnetic Resonance ImagingProcedure: Multigated Acquisition ScanOther: Placebo AdministrationOther: Quality-of-Life AssessmentProcedure: X-Ray Imaging

Interventions

Biospecimen Collectionprocedure

Undergo blood sample collection

Computed Tomographyprocedure

Undergo CT

Echocardiography Testprocedure

Undergo ECHO

Laboratory Biomarker Analysisother

Correlative studies

Magnetic Resonance Imagingprocedure

Undergo MRI

Multigated Acquisition Scanprocedure

Undergo MUGA

Pazopanib Hydrochloridedrug

Given PO

Placebo Administrationother

Given PO

Quality-of-Life Assessmentother

Ancillary studies

X-Ray Imagingprocedure

Undergo chest x-ray