NCT00041808

Brief Summary

MTC-DOX is Doxorubicin or DOX, a chemotherapy drug, that is adsorbed, or made to "stick", to magnetic beads (MTCs). MTCs are tiny, microscopic particles of iron and carbon. When DOX is added to MTCs, DOX attaches to the carbon part of the MTCs. MTC-DOX is directed to and deposited in the area of a tumor, where it is thought that it then "leaks" through the blood vessel walls. Once in the surrounding tissues, it is thought that Doxorubicin becomes "free from" the magnetic beads and will then be able to act against the tumor cells. The iron component of the particle has magnetic properties, making it possible to direct MTC-DOX to specific tumor sites in the liver by placing a magnet on the body surface. It is hoped that MTC-DOX used with the magnet may target the chemotherapy drug directly to liver tumors and provide a treatment to patients with cancers that have spread to the liver.

Trial Health

90
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at P25-P50 for phase_1

Timeline
Completed

Started Jul 2001

Geographic Reach
2 countries

4 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2001

Completed
1 year until next milestone

First Submitted

Initial submission to the registry

July 17, 2002

Completed
2 days until next milestone

First Posted

Study publicly available on registry

July 19, 2002

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2003

Completed
Last Updated

June 24, 2005

Status Verified

February 1, 2003

First QC Date

July 17, 2002

Last Update Submit

June 23, 2005

Conditions

Keywords

Metastatic liver cancerCholangiocarcinomacolorectal canceresophageal cancergastric cancerpancreatic cancerbreast cancermalignant melanomasarcomaGISTgastrointestinal stromal tumorlung cancerliver cancer

Interventions

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients with a Karnofsky (or equivalent) performance status \> 60 and an expected survival of \> 2 months
  • Patients agreeing to use a medically effective method of contraception
  • Patients able to understand and give written informed consent
  • The center of the tumor mass must be \< or = 14 cm from the anterior or lateral abdominal wall as determined by cross sectional imaging measured at baseline. This is required for optimal retention of MTC-DOX by the magnetic field. If more than one tumor mass is present, all of the treated tumor masses must meet this criterion

You may not qualify if:

  • Women who are pregnant or lactating
  • Patient's with metastatic liver cancer, or other primary liver cancer excluding HCC, with diffuse disease that does not have focal area(s) conducive to local regional therapy
  • Patients with the following laboratory abnormalities:Hemoglobin \< 10.0 g/dL;Granulocyte count \< 1,500 per mm3;Platelet count \< 50,000 per mm3; Lymphocyte count \< 0.5 x 10 to the 9th per L; Total bilirubin \>/= 3.0 mg/dL;AST or ALT \>/= 5x the upper limit of normal;INR \>/= 1.3; Creatinine \>/= 2.0 mg/dL
  • Patients with either significant cardiovascular disease or any other organ system dysfunction which, in the opinion of the investigator, would either compromise the patient's safety or interfere with the evaluation of the test material. Patients with evidence of a myocardial infarction within six (6) months prior to this trial will be excluded.
  • Patients with an indwelling cardiac pacemaker, cerebral aneurysm clips, or any other indwelling device or appliance that could be adversely affected by the use of the external magnet
  • Patients at the time of study entry with a second invasive cancer other than basal cell and squamous cell carcinoma of the skin, or carcinoma in situ of the cervix
  • Patients with documented evidence of hemachromatosis or hemosiderosis
  • Patients with CT or ultrasound evidence of portal vein invasion or thrombosis
  • Patients who have had prior anthracycline therapy with a left ventricular ejection fraction (LVEF) \<50%, as measured by either multigated radionuclide angiography (MUGA) scan or echocardiogram.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (4)

Scripps Stevens Cancer Division

San Diego, California, 92037, United States

Location

UCSF Cancer Center

San Francisco, California, 94143, United States

Location

Scott and White Clinic

Temple, Texas, 76508, United States

Location

Frankfurt Universtiy

Frankfurt, 60590, Germany

Location

MeSH Terms

Conditions

Neoplasm MetastasisColorectal NeoplasmsEsophageal NeoplasmsStomach NeoplasmsPancreatic NeoplasmsBreast NeoplasmsMelanomaSarcomaGastrointestinal NeoplasmsLung NeoplasmsLiver NeoplasmsCholangiocarcinomaGastrointestinal Stromal Tumors

Interventions

InjectionsDrug Therapy

Condition Hierarchy (Ancestors)

Neoplastic ProcessesNeoplasmsPathologic ProcessesPathological Conditions, Signs and SymptomsIntestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteDigestive System DiseasesGastrointestinal DiseasesColonic DiseasesIntestinal DiseasesRectal DiseasesHead and Neck NeoplasmsEsophageal DiseasesStomach DiseasesEndocrine Gland NeoplasmsPancreatic DiseasesEndocrine System DiseasesBreast DiseasesSkin DiseasesSkin and Connective Tissue DiseasesNeuroendocrine TumorsNeuroectodermal TumorsNeoplasms, Germ Cell and EmbryonalNeoplasms by Histologic TypeNeoplasms, Nerve TissueNevi and MelanomasSkin NeoplasmsNeoplasms, Connective and Soft TissueRespiratory Tract NeoplasmsThoracic NeoplasmsLung DiseasesRespiratory Tract DiseasesLiver DiseasesAdenocarcinomaCarcinomaNeoplasms, Glandular and EpithelialNeoplasms, Connective Tissue

Intervention Hierarchy (Ancestors)

Drug Administration RoutesTherapeutics

Study Officials

  • Joy Koda, PhD

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
INDUSTRY

Study Record Dates

First Submitted

July 17, 2002

First Posted

July 19, 2002

Study Start

July 1, 2001

Study Completion

April 1, 2003

Last Updated

June 24, 2005

Record last verified: 2003-02

Locations