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NCT01435122 · ClinicalTrials.gov registry record · Phase 2

A Study of Axitinib in Advanced Carcinoid Tumors

A Phase 2 study of Carcinoid Tumor, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

Completed
Registry status
Phase 2
Development phase
30
Enrollment target
2
Study locations

NCT01435122 is a Phase 2 study of Carcinoid Tumor that has completed, run by H. Lee Moffitt Cancer Center and Research Institute. The registered enrollment target is 30 participants, below the 95-participant average among 8 other Carcinoid Tumor trials with a reported enrollment target (68% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT01435122, a Phase 2 study of Carcinoid Tumor, has completed, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

COMPLETED
Registry status
Phase 2
Development phase
30 participants
Enrollment target
2
Study locations

Study Summary

The main purpose of this study is to see whether Axitinib will help prolong the time that the patient's carcinoid tumors remain stable, and to examine their treatment response through testing. Researchers also want to find out if Axitinib is safe and tolerable.

Conditions Studied

Interventions

  • DRUG Axitinib

Study Locations (2)

California

  • University of California San Francisco (UCSF) - San Francisco

Florida

  • H. Lee Moffitt Cancer Center and Research Institute - Tampa

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2011-10-25
Est. Completion 2018-02-13
Phase Phase 2

What the Registry Record Tells You About NCT01435122

The ClinicalTrials.gov registry entry for NCT01435122 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 95-participant average among 8 other Carcinoid Tumor trials with a reported enrollment target (68% lower). The listed sponsor is H. Lee Moffitt Cancer Center and Research Institute, which has 502 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Carcinoid Tumor appearing as the primary indexed condition, and to 1 intervention - of which Axitinib is the first listed.

NCT01435122 reports 2 study locations spanning 2 distinct geographic areas - top geographies include California, Florida.

Frequently Asked Questions

What is clinical trial NCT01435122 about?

NCT01435122 is a clinical study titled "A Study of Axitinib in Advanced Carcinoid Tumors". The main purpose of this study is to see whether Axitinib will help prolong the time that the patient's carcinoid tumors remain stable, and to examine their treatment response through testing. Researchers also want to find out if Axitinib is safe and tolerable.

What is the current status of trial NCT01435122?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2011-10-25. Estimated completion is 2018-02-13.

What conditions does trial NCT01435122 study?

This clinical trial studies the following conditions: Carcinoid Tumor.

What interventions are being tested in trial NCT01435122?

The interventions under investigation include: Axitinib (DRUG).

Who is sponsoring clinical trial NCT01435122?

This trial is sponsored by H. Lee Moffitt Cancer Center and Research Institute, which has 502 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01435122 being conducted?

This trial has 2 study locations across California, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.