Phase I, Open Label, Single Center Safety Study of [F-18]FLT

NCT ID: NCT00553748

Last Updated: 2008-07-03

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 11 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-11-30
• Study Completion Date: 2008-05-31

Brief Summary

This is a ten subject, phase 1 study. The purpose of the Phase 1 study is to demonstrate drug safety in a target group of subjects with high grade brain cancer. This population represents a potential clinical population that may benefit from this PET imaging tracer. The study will also begin collection of baseline imaging data and allow us to gain information to improve design and conduct of future trials.

Detailed Description

This is a ten subject, phase 1 study. The purpose of the study is to demonstrate drug safety in a group with high grade brain tumors and to evaluate cell proliferation with F-18 FLT. FLT is known to clear out of normal brain and detect brain tumor. This population represents a potential clinical population that may benefit from this PET imaging tracer. This information will help improve the design and conduct of future F-18 FLT clinical trials.

Conditions

Brain Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

I

Group Type: EXPERIMENTAL

F-18 FLT

Intervention Type: DRUG

One - 10 mci dose of F-18 FLT is administered IV over about 5 seconds prior to PET imaging. Each imaging dose contains no more than 6.1 micrograms of FLT.

Interventions

F-18 FLT

One - 10 mci dose of F-18 FLT is administered IV over about 5 seconds prior to PET imaging. Each imaging dose contains no more than 6.1 micrograms of FLT.

Intervention Type: DRUG

Other Intervention Names

18-F FLT; [F-18]FLT

Eligibility Criteria

Inclusion Criteria

• Subject may be male or female and of any race / ethnicity;
• At the time of study drug dosing, the subject has reached his or her 18th birthday;
• Subject has histologic diagnosis of one of the following malignancies - glioblastoma gliosarcoma, anaplastic mixed/anaplastic oligodendroglioma or (anaplastic) astrocytoma with lesion visible on CT or MR and minimum histological grade of III/IV;
• Subject with suspect radiation necrosis that are planned for re-section;
• Subject or subject's legally acceptable representative provides informed consent;
• Subject is capable of complying with study procedures and able to lie still in the PET scanner;
• Subject is capable of communicating with study personnel;
• Subject has adequate liver and kidney function

Exclusion Criteria

• Subject is pregnant or nursing;
• Subject is anemic (as defined as a hemoglobin level <10);
• Subject has not received chemotherapy or radiation therapy within the two weeks prior to imaging.
• Subject has as reflected by a serum liver enzymes outside the normal laboratory reference range;
• Subject has a history of chronic liver disease, which may compromise liver function;
• Subject has kidney disease as reflected by a serum creatinine outside the normal laboratory reference range;
• Subject has prior history of stroke or other condition of the head or neck that, in the investigator's opinion, might affect circulation to the brain or image interpretation (examples include, but are not limited to, previous stroke with cystic softening and cerebral deformity, or arteriovenous malformation);
• Subject has a history of significant cerebrovascular disease;
• Subject has any other condition or personal circumstance that, in the judgment of the investigator, might interfere with the collection of complete good quality data
• Subject has previously received [F-18]FLT at any time, or any other investigational product within the past two weeks.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Siemens Molecular Imaging

INDUSTRY

Sponsor Role: lead

Responsible Party

Thomas Jefferson University

Principal Investigators

Charles M Intenzo, MD

Role: PRINCIPAL_INVESTIGATOR

Thomas Jefferson University Hospital, 132 S 10th St Phila, PA 19107

Locations

Thomas Jefferson University Hospital

Philadelphia, Pennsylvania, United States

Countries

United States

Other Identifiers

D0008186

Identifier Type: -

Identifier Source: org_study_id