Magnetic-Targeted Doxorubicin in Treating Patients With Cancer Metastatic to the Liver
A Phase I/II Single Dose Trial to Determine The Safety, Tolerance, Pharmacokinetic Profile, and Preliminary Activity of Intrahepatic Delivery (Via Hepatic Artery Catheterization) of Doxorubicin Hydrochloride Adsorbed to Magnetic Targeted Carriers ( MTC-DOX) in Patients With Metastatic Cancer to the Liver .
1 other identifier
interventional
20
2 countries
4
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_1
Started Jul 2001
4 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2001
CompletedFirst Submitted
Initial submission to the registry
July 17, 2002
CompletedFirst Posted
Study publicly available on registry
July 19, 2002
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2003
CompletedJune 24, 2005
February 1, 2003
July 17, 2002
June 23, 2005
Conditions
Keywords
Interventions
Eligibility Criteria
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
- FeRxlead
Study Sites (4)
Scripps Stevens Cancer Division
San Diego, California, 92037, United States
UCSF Cancer Center
San Francisco, California, 94143, United States
Scott and White Clinic
Temple, Texas, 76508, United States
Frankfurt Universtiy
Frankfurt, 60590, Germany
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Joy Koda, PhD
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