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NCT00082823 · ClinicalTrials.gov registry record · Phase 1

Intravenous VEGF Trap in Treating Patients With Relapsed or Refractory Advanced Solid Tumors or Non-Hodgkin's Lymphoma

A Phase 1 study of Cancer, sponsored by Regeneron Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
25
Enrollment target
2
Study locations

NCT00082823 is a Phase 1 study of Cancer that has completed, run by Regeneron Pharmaceuticals. The registered enrollment target is 25 participants, below the 3,491-participant average among 615 other Cancer trials with a reported enrollment target (99% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT00082823, a Phase 1 study of Cancer, has completed, sponsored by Regeneron Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
25 participants
Enrollment target
2
Study locations

Study Summary

RATIONALE: Intravenous VEGF Trap may stop the growth of solid tumors or non-Hodgkin's lymphoma by stopping blood flow to the cancer. PURPOSE: This phase I trial is studying the side effects of VEGF Trap in treating patients with relapsed or refractory advanced solid tumors or non-Hodgkin's lymphoma.

Conditions Studied

Interventions

  • BIOLOGICAL ziv-aflibercept

Study Locations (2)

New York

  • Memorial Sloan - Kettering Cancer Center - New York

Tennessee

  • Vanderbilt-Ingram Cancer Center - Nashville

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2004-01
Phase Phase 1

Sponsor

Regeneron Pharmaceuticals

280 total trials

What the Registry Record Tells You About NCT00082823

The ClinicalTrials.gov registry entry for NCT00082823 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,491-participant average among 615 other Cancer trials with a reported enrollment target (99% lower). The listed sponsor is Regeneron Pharmaceuticals, which has 280 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Cancer appearing as the primary indexed condition, and to 1 intervention - of which ziv-aflibercept is the first listed.

NCT00082823 reports 2 study locations spanning 2 distinct geographic areas - top geographies include New York, Tennessee.

Frequently Asked Questions

What is clinical trial NCT00082823 about?

NCT00082823 is a clinical study titled "Intravenous VEGF Trap in Treating Patients With Relapsed or Refractory Advanced Solid Tumors or Non-Hodgkin's Lymphoma". RATIONALE: Intravenous VEGF Trap may stop the growth of solid tumors or non-Hodgkin's lymphoma by stopping blood flow to the cancer. PURPOSE: This phase I trial is studying the side effects of VEGF Trap in treating patients with relapsed or refractory advanced solid tumors or non-Hodgkin's lymphoma...

What is the current status of trial NCT00082823?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2004-01.

What conditions does trial NCT00082823 study?

This clinical trial studies the following conditions: Cancer.

What interventions are being tested in trial NCT00082823?

The interventions under investigation include: ziv-aflibercept (BIOLOGICAL).

Who is sponsoring clinical trial NCT00082823?

This trial is sponsored by Regeneron Pharmaceuticals, which has 280 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00082823 being conducted?

This trial has 2 study locations across New York, Tennessee. 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

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.