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NCT00257465 · ClinicalTrials.gov registry record · Phase 1

Trial of Autologous, Hapten-Modified Vaccine in Patients With Stage III or IV Melanoma

A Phase 1 study of Melanoma, sponsored by AVAX Technologies.

Completed
Registry status
Phase 1
Development phase
82
Enrollment target
7
Study locations

NCT00257465 is a Phase 1 study of Melanoma that has completed, run by AVAX Technologies. The registered enrollment target is 82 participants, below the 706-participant average among 266 other Melanoma trials with a reported enrollment target (88% lower). The trial reports 7 study locations across 6 states.

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The verdict

NCT00257465, a Phase 1 study of Melanoma, has completed, sponsored by AVAX Technologies.

COMPLETED
Registry status
Phase 1
Development phase
82 participants
Enrollment target
7
Study locations

Study Summary

The purpose of this study is to determine whether a vaccine composed of patients' own melanoma cells treated with the chemical, dinitrophenyl (DNP)(called a hapten), is safe and stimulates an immune response to patients' own cancer cells.

Conditions Studied

Interventions

  • BIOLOGICAL Autologous, DNP-modified vaccine (M-Vax)
  • BIOLOGICAL Autologous, DNP-Modified Melanoma Vaccine
  • BIOLOGICAL Autologous, DNP-Modified Vaccine

Study Locations (7)

Pennsylvania

  • Hospital of the University of Pennsylvania - Philadelphia
  • Thomas Jefferson University - Philadelphia

Arizona

  • University of Arizona Cancer Center - Tucson

California

  • Pacific Oncology and Hematology Associates - San Diego

Illinois

  • University of Illinois School of Medicine - Chicago

Kentucky

  • University of Louisville - Louisville

Texas

  • MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 82 participants
Start Date 2005-06
Est. Completion 2008-06
Phase Phase 1

Sponsor

AVAX Technologies

3 total trials

What the Registry Record Tells You About NCT00257465

The ClinicalTrials.gov registry entry for NCT00257465 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 82 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 706-participant average among 266 other Melanoma trials with a reported enrollment target (88% lower). The listed sponsor is AVAX Technologies, which has 3 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Melanoma appearing as the primary indexed condition, and to 3 interventions - of which Autologous, DNP-modified vaccine (M-Vax) is the first listed.

NCT00257465 reports 7 study locations spanning 6 distinct geographic areas - top geographies include Pennsylvania, Arizona, California.

Frequently Asked Questions

What is clinical trial NCT00257465 about?

NCT00257465 is a clinical study titled "Trial of Autologous, Hapten-Modified Vaccine in Patients With Stage III or IV Melanoma". The purpose of this study is to determine whether a vaccine composed of patients' own melanoma cells treated with the chemical, dinitrophenyl (DNP)(called a hapten), is safe and stimulates an immune response to patients' own cancer cells.

What is the current status of trial NCT00257465?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 82 participants. The study started on 2005-06. Estimated completion is 2008-06.

What conditions does trial NCT00257465 study?

This clinical trial studies the following conditions: Melanoma.

What interventions are being tested in trial NCT00257465?

The interventions under investigation include: Autologous, DNP-modified vaccine (M-Vax) (BIOLOGICAL), Autologous, DNP-Modified Melanoma Vaccine (BIOLOGICAL), Autologous, DNP-Modified Vaccine (BIOLOGICAL).

Who is sponsoring clinical trial NCT00257465?

This trial is sponsored by AVAX Technologies, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00257465 being conducted?

This trial has 7 study locations across Arizona, California, Illinois, Kentucky, Pennsylvania. 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.