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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
BioMed Valley Discoveries, Inc
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

The following are the main inclusion criteria for all subjects:

  1. Males or females age > 18 years
  2. Informed consent
  3. Subjects with chronic medical conditions such as hypertension and diabetes should be considered stable by the principal investigator
  4. Women should be postmenopausal or surgically sterile
  5. Able to return for all study assessments

In addition, the following main inclusion criteria apply for subjects with suspected prosthetic joint infection:

  1. Operative intervention planned in the 30 days following study enrollment
  2. Prosthetic joint implant in site for more than 3 months prior to enrollment

The following are the main exclusion criteria for all subjects:

  1. Unable to comply with study requirements
  2. Indication in the opinion of the principal investigator for surgery within 48 hours of presentation.
  3. Receipt of any antibiotic therapy in the 2 weeks preceding imaging
  4. 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
  5. Requirement for any medication that predisposes to lactic acidosis (e.g., metformin, iron, isoniazid and salicylates; see Appendix A)
  6. Requirement for any medication that has potential mitochondrial toxicity, e.g., nucleoside analogues (zidovudine, didanosine, stavudine)
  7. 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]
  8. Chronic hepatitis B virus (HBV) or hepatitis C virus (HCV) infection
  9. Pre-existing myopathy or neuropathy
  10. Abnormal liver function tests defined as alanine aminotransferase (ALT) > the upper limit of normal (ULN), aspartate aminotransferase (AST) > ULN, gamma glutamyl transferase (GGT) > ULN
  11. Alcohol use > 3 units per day in men or 2 units per day in women or active intravenous drug use
  12. Creatinine clearance < 30 mL/min
  13. Body mass index > 40
  14. Life expectancy < 6 months
  15. 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

First Posted
April 8, 2011
Last Updated
June 26, 2013
Sponsor
BioMed Valley Discoveries, Inc
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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

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Biodistribution and Dosimetry Evaluation of [124I]FIAU

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