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Type 1 DiabetesPhase 1NCT01515384

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

A Phase 1 study testing 18F-AV-133 in people with Type 1 Diabetes and Type 2 Diabetes, run by Avid Radiopharmaceuticals at 1 site in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

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

Who is it for?
Ages 18 to 70 yearsHealthy volunteers can take part
Conditions the study is for
Type 1 Diabetes, Type 2 Diabetes
What is being tested?
18F-AV-133
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
19 participants
Where
1 siteUnited States
Study dates
Jun 2010to Feb 2013
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 70 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

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.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Research Site

    New York, New York, 10027

Other trials in United States

About this study

Official title: 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

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

Read the 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.
Being tested
18F-AV-133
Medical subject headings
Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • 18F-AV-133Drug

    IV injection, 7.6 mCi (281.2 MBq)

Study groups in NCT01515384
Study groupRoleWhat they receive
Type 1 DiabetesExperimentalNot described
Receives: Drug: 18F-AV-133
Type 2 DiabetesExperimentalNot described
Receives: Drug: 18F-AV-133
Healthy ControlsExperimentalNot described
Receives: Drug: 18F-AV-133

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pancreatic uptake and clearance of 18F-AV-133 tracer as determined by SUVR

    SUVR=standard uptake value ratio

    Measured: 0-90 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jan 2012 (estimated)
  2. Study startJun 2010
  3. Primary completionFeb 2013
  4. Study completionFeb 2013

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Diagnosis
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
19 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01515384
Sponsor's protocol ID
18F-AV-133-D01
Status last verified
Jan 2020
First submitted
21 Feb 2011
Last updated
13 Jan 2020
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing 18F-AV-133 in people with Type 1 Diabetes and Type 2 Diabetes, run by Avid Radiopharmaceuticals at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 13 Jan 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study was stopped early. Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pancreatic uptake and clearance of 18F-AV-133 tracer as determined by SUVR (time frame: 0-90 minutes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Jan 2020.

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