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A Trial of 18F-AV-133 Positron Emission Tomography (PET)

A Preliminary Evaluation of the Safety and Pancreas Imaging Properties of 18F-AV-133 in Healthy Volunteers and in Patients With Type 1 or Type 2 Diabetes

Status
Terminated
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01515384
Enrollment
19
Registered
2012-01-24
Start date
2010-06-30
Completion date
2013-02-28
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 Diabetes, Type 2 Diabetes

Brief summary

The purpose of this study is to evaluate the safety and pancreas imaging properties of 18F-AV-133.

Detailed description

The primary objective of this protocol is to address the feasibility for further development of the VMAT2-binding compound 18F-AV-133 as a diagnostic radiopharmaceutical in the field of diabetes. Specifically, this study will evaluate 18F-AV-133 imaging in patients with type 1 diabetes, patients with type 2 diabetes and in healthy controls in order to: 1. Obtain information regarding the safety of 18F-AV-133 in these populations; 2. Determine whether uptake, distribution, or clearance of 18F-AV-133 in the pancreas differs between subjects with predicted reduced beta cell mass (patients with type 1 or type 2 diabetes of long duration) and normal beta cell mass (healthy volunteers); 3. Evaluate the PET imaging pharmacokinetics of 18F-AV-133 in abdominal organs of healthy control subjects and patients with type 1 or type 2 diabetes; 4. Obtain preliminary information regarding the appropriate time window for optimal PET imaging of 18F-AV-133 in the pancreas post-administration for type 1, type 2, and normal healthy individuals; 5. Obtain preliminary information regarding an appropriate reference tissue for evaluating the PET imaging results of 18F-AV-133 in the pancreas; and 6. Evaluate the imaging properties of 18F-AV-133 in the pancreas relative to the brain in a subset of subjects.

Interventions

IV injection, 7.6 mCi (281.2 MBq)

Sponsors

Avid Radiopharmaceuticals
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

Patients with type 1 diabetes may be enrolled if they meet all of the following criteria: * Are males or females between 18 and 70 years of age, inclusive; * Have a diagnosis of type 1 diabetes mellitus as defined by ADA criteria; diabetes onset younger than age 21, duration \>5 years; Insulin dose requirements ≤ 0.8 units/kg/day; * HbA1c level ≥ 5% and ≤ 8%; * Have fasting C-Peptide \< 0.1 ng/ml; * Have a BMI between 18 and 32 kg/m2; * Able to tolerate PET imaging; * In the judgment of the physician, are capable of fasting 4-6 hours prior to screening and Day 1 imaging procedures; and * Give informed consent. Patients with type 2 diabetes may be enrolled if they meet all of the following criteria: * Are males or females between 18 and 70 years of age, inclusive; * Must have been diagnosed with type 2 diabetes for more than five years; * HbA1c level ≥ 5% and ≤ 8%; * Have a BMI between 18 and 32 kg/m2; * Glucose \> 200 mg/dl on Mixed Meal Tolerance Test at screening visit; * Able to tolerate PET imaging; * In the judgment of the physician, are capable of fasting 4-6 hours prior to screening and Day 1 imaging procedures; and * Give informed consent. Healthy volunteers may be enrolled if they meet all of the following criteria: * Are males or females between 18 and 70 years of age, inclusive; * Have no history of type 1 or type 2 diabetes in a first degree relative; * Fasting blood glucose ≤ 100 mg/dL; * HbA1c level ≤ 6%; * Normal Mixed Meal Tolerance test at screening visit; * BMI between 18 and 32 kg/m2; * Able to tolerate PET imaging; * In the judgment of the physician, are capable of fasting 4-6 hours prior to screening and Day 1 imaging procedures; and * Give informed consent. Subjects will be excluded from enrollment if they meet any of the following criteria: * Clinically significant renal dysfunction; * Clinically significant liver dysfunction as determined by history, physical examination, and standard liver function testing at screening (AST, ALT, Total/Direct Bilirubin, Alkaline Phosphatase); * Coagulopathy; * Use medications known to affect dopaminergic function, including MAO inhibitors, tetrabenazine, or levodopa; * Recent (within 3 months) or current treatment with drugs influencing beta cell function or insulin sensitivity (e.g. glucocorticoids, reserpine); * Have polycystic ovarian syndrome; * History of movement disorder such as Parkinson's Disease, Huntington's Disease; * Clinically significant psychiatric disease or history of psychiatric illness such as depression, bipolar disease, anxiety or schizophrenia; * Current use (within past year) of cocaine, methamphetamine, and/or ecstasy ( MDMA, 34- methylenedioxymethamphetamine; * Have a recent history of alcohol or substance abuse or dependence; * Clinically significant cardiovascular disease or clinically significant abnormalities on screening ECG (including but not limited to QTc\>450 msec); * Clinically significant pulmonary, renal or hepatic impairment, or cancer; * Have clinically significant infectious disease, including AIDS or HIV infection or previous positive test for hepatitis B, hepatitis C, HIV-1, or HIV-2; * Are women of childbearing potential who are not surgically sterile, not refraining from sexual activity or not using adequate contraception. Women must not be pregnant (negative serum β-HCG at the time of screen) or breastfeeding at screening, and must agree to take appropriate steps not to become pregnant for 30 days following the clinical trial; * Require medications with a narrow therapeutic window (e.g., warfarin), are receiving any investigational medications, or have participated in a trial with investigational medications within the last 30 days; * Weigh more than the manufacturer-recommended limit for the PET/CT camera being used; * Any prior participation in other research protocols within the past month that involved radiation, with the exception of plain radiography studies (i.e., chest x-rays); and * Have received a diagnostic or therapeutic radiopharmaceutical within the past week.

Design outcomes

Primary

MeasureTime frameDescription
Pancreatic uptake and clearance of 18F-AV-133 tracer as determined by SUVR0-90 minutesSUVR=standard uptake value ratio

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026