Biodistribution and Dosimetry Evaluation of [124I]FIAU
Primary Purpose
Prosthesis Related Infections
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
[124I]FIAU
Sponsored by
About this trial
This is an interventional diagnostic trial for Prosthesis Related Infections focused on measuring Phase I, FIAU, Fialuridine, Biodistribution, Dosimetry, Prosthetic, Joint, Infection, PET-CT
Eligibility Criteria
The following are the main inclusion criteria for all subjects:
- Males or females age > 18 years
- Informed consent
- Subjects with chronic medical conditions such as hypertension and diabetes should be considered stable by the principal investigator
- Women should be postmenopausal or surgically sterile
- Able to return for all study assessments
In addition, the following main inclusion criteria apply for subjects with suspected prosthetic joint infection:
- Operative intervention planned in the 30 days following study enrollment
- Prosthetic joint implant in site for more than 3 months prior to enrollment
The following are the main exclusion criteria for all subjects:
- Unable to comply with study requirements
- Indication in the opinion of the principal investigator for surgery within 48 hours of presentation.
- Receipt of any antibiotic therapy in the 2 weeks preceding imaging
- Immunosuppression, e.g., human immunodeficiency virus (HIV) infection, s/p organ transplantation, receipt of steroids for > 10 days at > 10 mg of prednisone equivalent daily within the 90 days prior to enrollment
- Requirement for any medication that predisposes to lactic acidosis (e.g., metformin, iron, isoniazid and salicylates; see Appendix A)
- Requirement for any medication that has potential mitochondrial toxicity, e.g., nucleoside analogues (zidovudine, didanosine, stavudine)
- History of an inherited mitochondrial disorder (e.g., Leber's hereditary neuropathy, neuropathy, ataxia, retinitis pigmentosa and ptosis [NARP], myoneurogenic gastrointestinal encephalopathy [MNGIE], myoclonic epilepsy with ragged red fibers [MERFF] and mitochondrial myopathy, encephalomyopathy, lactic acidosis and stroke-like syndrome [MELAS]
- Chronic hepatitis B virus (HBV) or hepatitis C virus (HCV) infection
- Pre-existing myopathy or neuropathy
- Abnormal liver function tests defined as alanine aminotransferase (ALT) > the upper limit of normal (ULN), aspartate aminotransferase (AST) > ULN, gamma glutamyl transferase (GGT) > ULN
- Alcohol use > 3 units per day in men or 2 units per day in women or active intravenous drug use
- Creatinine clearance < 30 mL/min
- Body mass index > 40
- Life expectancy < 6 months
- Hypersensitivity to iodine
Sites / Locations
- University of Arkansas for Medical Sciences
- Sinai Hospital of Baltimore
- North Shore long Island Jewish Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
[124I]FIAU
Arm Description
single dose study of [124I]FIAU in healthy volunteers or subjects with prosthetic joint infection who will undergo PET-CT scanning
Outcomes
Primary Outcome Measures
Determine the biodistribution and dosimetry evaluation of [124I]FIAU
Subjects will be dosed with [124I]FIAU at Time 0 on Day 0, and a PET-CT scan will be conducted immediately after the injection. Imaging will be repeated at 2 hours, 4 hours, 6 hours, 24 hours, 48 hours, and 72 hours after dosing.
All images generated will be reviewed for biodistribution and dosimetry.
Secondary Outcome Measures
Evaluate the safety and tolerability of [124I]FIAU
Safety will be monitored throughout the study for all subjects. Safety will be assessed by monitoring of adverse events and vital signs, clinical laboratory tests including LFTs, lactate, serum chemistry and CBC, physical examination, and 12-lead ECG.
Full Information
NCT ID
NCT01337466
First Posted
April 8, 2011
Last Updated
June 26, 2013
Sponsor
BioMed Valley Discoveries, Inc
1. Study Identification
Unique Protocol Identification Number
NCT01337466
Brief Title
Biodistribution and Dosimetry Evaluation of [124I]FIAU
Official Title
Biodistribution and Dosimetry of [124i]FIAU in Patients With Prosthetic Joint Infection of The Knee or Hip and Healthy Subjects Using PET-CT Scanning
Study Type
Interventional
2. Study Status
Record Verification Date
June 2013
Overall Recruitment Status
Completed
Study Start Date
December 2010 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
March 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
BioMed Valley Discoveries, Inc
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This protocol will evaluate the biodistribution and dosimetry of [124I]FIAU in both healthy volunteers and patients with prosthetic joint infections. This pilot study will also investigate the safety and tolerability of [124I]FIAU.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prosthesis Related Infections
Keywords
Phase I, FIAU, Fialuridine, Biodistribution, Dosimetry, Prosthetic, Joint, Infection, PET-CT
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
[124I]FIAU
Arm Type
Experimental
Arm Description
single dose study of [124I]FIAU in healthy volunteers or subjects with prosthetic joint infection who will undergo PET-CT scanning
Intervention Type
Radiation
Intervention Name(s)
[124I]FIAU
Other Intervention Name(s)
Fialuridine
Intervention Description
This is a single dose study of 2 mCi [124I]FIAU in healthy volunteers or subjects with prosthetic joint infection of the knee or hip who will undergo serial PET-CT scanning.
Primary Outcome Measure Information:
Title
Determine the biodistribution and dosimetry evaluation of [124I]FIAU
Description
Subjects will be dosed with [124I]FIAU at Time 0 on Day 0, and a PET-CT scan will be conducted immediately after the injection. Imaging will be repeated at 2 hours, 4 hours, 6 hours, 24 hours, 48 hours, and 72 hours after dosing.
All images generated will be reviewed for biodistribution and dosimetry.
Time Frame
72 hrs
Secondary Outcome Measure Information:
Title
Evaluate the safety and tolerability of [124I]FIAU
Description
Safety will be monitored throughout the study for all subjects. Safety will be assessed by monitoring of adverse events and vital signs, clinical laboratory tests including LFTs, lactate, serum chemistry and CBC, physical examination, and 12-lead ECG.
Time Frame
28 +/- 2 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
The following are the main inclusion criteria for all subjects:
Males or females age > 18 years
Informed consent
Subjects with chronic medical conditions such as hypertension and diabetes should be considered stable by the principal investigator
Women should be postmenopausal or surgically sterile
Able to return for all study assessments
In addition, the following main inclusion criteria apply for subjects with suspected prosthetic joint infection:
Operative intervention planned in the 30 days following study enrollment
Prosthetic joint implant in site for more than 3 months prior to enrollment
The following are the main exclusion criteria for all subjects:
Unable to comply with study requirements
Indication in the opinion of the principal investigator for surgery within 48 hours of presentation.
Receipt of any antibiotic therapy in the 2 weeks preceding imaging
Immunosuppression, e.g., human immunodeficiency virus (HIV) infection, s/p organ transplantation, receipt of steroids for > 10 days at > 10 mg of prednisone equivalent daily within the 90 days prior to enrollment
Requirement for any medication that predisposes to lactic acidosis (e.g., metformin, iron, isoniazid and salicylates; see Appendix A)
Requirement for any medication that has potential mitochondrial toxicity, e.g., nucleoside analogues (zidovudine, didanosine, stavudine)
History of an inherited mitochondrial disorder (e.g., Leber's hereditary neuropathy, neuropathy, ataxia, retinitis pigmentosa and ptosis [NARP], myoneurogenic gastrointestinal encephalopathy [MNGIE], myoclonic epilepsy with ragged red fibers [MERFF] and mitochondrial myopathy, encephalomyopathy, lactic acidosis and stroke-like syndrome [MELAS]
Chronic hepatitis B virus (HBV) or hepatitis C virus (HCV) infection
Pre-existing myopathy or neuropathy
Abnormal liver function tests defined as alanine aminotransferase (ALT) > the upper limit of normal (ULN), aspartate aminotransferase (AST) > ULN, gamma glutamyl transferase (GGT) > ULN
Alcohol use > 3 units per day in men or 2 units per day in women or active intravenous drug use
Creatinine clearance < 30 mL/min
Body mass index > 40
Life expectancy < 6 months
Hypersensitivity to iodine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael A Mont, MD
Organizational Affiliation
Sinai Hospital of Baltimore
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Arkansas for Medical Sciences
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72205
Country
United States
Facility Name
Sinai Hospital of Baltimore
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21215
Country
United States
Facility Name
North Shore long Island Jewish Medical Center
City
Lake Success
State/Province
New York
ZIP/Postal Code
11042
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Biodistribution and Dosimetry Evaluation of [124I]FIAU
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