Imaging of Intravenous (IV) Combidex to Brain, Intra-cerebral Tumors and in Central Nervous System (CNS) Inflammation

This study has been terminated.
(AMAG not continuing with Combidex, the study drug)
Sponsor:
Collaborators:
Information provided by (Responsible Party):
OHSU Knight Cancer Institute
ClinicalTrials.gov Identifier:
NCT00659334
First received: April 10, 2008
Last updated: October 10, 2012
Last verified: October 2012
  Purpose

Combidex (ferumoxtran-10) is an ultra-small iron oxide particle covered with a sugar coating. It has been evaluated as an MRI contrast agent for use in imaging well perfused organs such as the liver and spleen and for imaging lymph nodes. In this study, Combidex is being used to compare the standard imaging agent, Gadolinium, in imaging brain tumors and the area adjacent to the tumor location. Combidex may provide the ability to better see brain tumors and inflammatory lesions on magnetic resonance imaging (MRI) scans. Combidex may be useful in its ability to cross blood vessels into brain tumors, and because of its size and ability to get into the area next to brain tumors, could assist in the treatment of brain tumors with other drugs in the future.


Condition Intervention Phase
Brain Neoplasms
Drug: Ferumoxtran-10 (Combidex)
Procedure: Neurosurgery
Phase 2

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Diagnostic
Official Title: Multi-disciplinary Study: MR, Histologic and EM Imaging of Intravenous Superparamagnetic Crystalline Particles (Combidex) to Brain, Intra-cerebral Tumors and in CNS Inflammation

Resource links provided by NLM:


Further study details as provided by OHSU Knight Cancer Institute:

Primary Outcome Measures:
  • Number of Participants Who Experience Optimal Imaging in Adult and Pediatric Brain Tumors to Establish Timing and Sequencing Parameters of Combidex. [ Time Frame: 24 hours (some patients between 3 and 72 hours) after administration of Combidex ] [ Designated as safety issue: No ]
    Signal intensity change in participants with Pre and 24 hours Post Combidex on T1, T2, T2* MRI sequences will be assessed (some patients undergo scans at 3 and 72 hours in order to assess radiographic changes at these time points). Combidex will be administered in dose 2.6 mg/kg in adults with high and low grade gliomas, metastases, meningiomas, and PNET; and in pediatric patients with astrocytomas grade i-iv, brain stem gliomas, ependymomas, CNS germ cell tumors, and PNET.


Secondary Outcome Measures:
  • Assess the Cellular Uptake of Particles in Brain Tumor Patients by Comparing Imaging Results With Histology and Electron Microscopic Examination of Biopsy Tissue [ Time Frame: 2 years ] [ Designated as safety issue: No ]
  • Compare Combidex Imaging in Brain Tumor Patients, With Other CNS Inflammatory Lesions Such as Multiple Sclerosis and Stroke. [ Time Frame: 2 years ] [ Designated as safety issue: No ]
  • Compare Pre- and Post-op Gd Enhanced MRI Combidex Enhanced MR Imaging Done Pre-, Intra- and Post-operatively, to Assess the Degree of Resection and Residual Tumor. [ Time Frame: 2 years ] [ Designated as safety issue: No ]

Enrollment: 116
Study Start Date: August 2000
Study Completion Date: March 2010
Primary Completion Date: March 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: 1
Adults with brain tumor to receive Combidex infusion only
Drug: Ferumoxtran-10 (Combidex)
2.6 mg/kg
Other Name: Combidex
Active Comparator: 2
Adults with brain tumors to receive Combidex infusion and neurosurgery
Drug: Ferumoxtran-10 (Combidex)
2.6 mg/kg
Other Name: Combidex
Procedure: Neurosurgery
neuro-surgical tumor biopsy or resection to assess particle localization. Biopsy (stereotactic, when possible) will take place following the 24 hour post- Combidex MR and within 48 hrs of i.v. Combidex administration. Biopsies will be taken from the tumor, brain around tumor (BAT) and brain distant to tumor and the MR localization and histology will be compared. The tissue will be obtained by either resection or needle frameless stereotactic biopsy.
3
Adults with brain tumors to receive neurosurgery only (NO Combidex)
Procedure: Neurosurgery
neuro-surgical tumor biopsy or resection to assess particle localization. Biopsy (stereotactic, when possible) will take place following the 24 hour post- Combidex MR and within 48 hrs of i.v. Combidex administration. Biopsies will be taken from the tumor, brain around tumor (BAT) and brain distant to tumor and the MR localization and histology will be compared. The tissue will be obtained by either resection or needle frameless stereotactic biopsy.
Active Comparator: 4
Children with brain tumors to receive Combidex only
Drug: Ferumoxtran-10 (Combidex)
2.6 mg/kg
Other Name: Combidex
Active Comparator: 5
Children with brain tumors to receive Combidex and neurosurgery
Drug: Ferumoxtran-10 (Combidex)
2.6 mg/kg
Other Name: Combidex
Procedure: Neurosurgery
neuro-surgical tumor biopsy or resection to assess particle localization. Biopsy (stereotactic, when possible) will take place following the 24 hour post- Combidex MR and within 48 hrs of i.v. Combidex administration. Biopsies will be taken from the tumor, brain around tumor (BAT) and brain distant to tumor and the MR localization and histology will be compared. The tissue will be obtained by either resection or needle frameless stereotactic biopsy.
6
Children with brain tumors to receive neurosurgery only, NO Combidex
Procedure: Neurosurgery
neuro-surgical tumor biopsy or resection to assess particle localization. Biopsy (stereotactic, when possible) will take place following the 24 hour post- Combidex MR and within 48 hrs of i.v. Combidex administration. Biopsies will be taken from the tumor, brain around tumor (BAT) and brain distant to tumor and the MR localization and histology will be compared. The tissue will be obtained by either resection or needle frameless stereotactic biopsy.
Active Comparator: 7
Adults with Inflammatory lesions (stroke or MS) to receive Combidex only
Drug: Ferumoxtran-10 (Combidex)
2.6 mg/kg
Other Name: Combidex

Detailed Description:

Subjects are recruited as patients in one of the neurology, neurosurgery or neuro-oncology clinics at OHSU. There are four groups of the study:

  • Subjects receive the combidex infusion only.
  • Subjects receive Combidex and undergo a previously schedule neurosurgery.
  • Subjects undergo surgery only and provide a sample of their tumor tissue to be used in pathology studies of Combidex.
  • Subjects with MS or stroke are invited to participate in receiving Combidex to evaluate the effectiveness of enhancing the area of damage within the brain.

Subjects are deemed eligible for the study and undergo a baseline MRI within 28 days of receiving Combidex. Subjects receiving Combidex are admitted for a half day into the Oregon Clinical & Translational Research Institute(OCTRI). Combidex is infused I.V. over 30 minutes. Subjects are monitored for side effects and are discharged within about 5 hours after the infusion, if no complications have been noted. Subjects return 24 hours after the infusion for a post infusion MRI scan and return again to one of the neurology clinics for one month follow-up. Subjects enrolled in group 2 undergo surgery 1-2 days after the Combidex infusion and also undergo a 24 post infusion MRI and return for one month follow-up. These subjects are also followed closely by the neurosurgical physician during the course of follow-up. Subjects enrolled in group 3 only undergo surgery and agree to have a piece of their tumor resection or biopsy donated for use in the study. Group 4 is the same as group 1, except the patient population includes multiple sclerosis and stroke instead of patients with brain tumors.

  Eligibility

Ages Eligible for Study:   5 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Brain tumor or CNS inflammatory lesion including stroke or MS
  • 5 yrs old or older
  • Able to undergo MRI without general anesthesia
  • Agree to be followed for 1 month following infusion of Combidex
  • Sign a written informed consent
  • If female and of child-bearing potential, be postmenopausal, sterile, or be on birth control for 1 month prior to study
  • Must have a pre-treatment MRI within 28 days before study

Exclusion Criteria:

  • Clinically significant signs of uncal herniation
  • Allergy to study drug, Combidex
  • Hepatic insufficiency
  • Stage IV or V renal insufficiency
  • If female, pregnant or lactating
  • Require anesthesia for MRI scanning
  • Hemachromatosis
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00659334

Locations
United States, Oregon
Oregon Health & Science University
Portland, Oregon, United States, 97239
Sponsors and Collaborators
OHSU Knight Cancer Institute
Investigators
Principal Investigator: Edward A Neuwelt, MD Oregon Health and Science University
  More Information

No publications provided

Responsible Party: OHSU Knight Cancer Institute
ClinicalTrials.gov Identifier: NCT00659334     History of Changes
Other Study ID Numbers: OHSU-1127, 5R01NS034608
Study First Received: April 10, 2008
Results First Received: May 15, 2012
Last Updated: October 10, 2012
Health Authority: United States: Food and Drug Administration

Keywords provided by OHSU Knight Cancer Institute:
Combidex
Diagnostic imaging

Additional relevant MeSH terms:
Brain Neoplasms
Neoplasms
Inflammation
Central Nervous System Neoplasms
Nervous System Neoplasms
Neoplasms by Site
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Pathologic Processes

ClinicalTrials.gov processed this record on July 22, 2014