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Effect of Gelofusine on GLP1-receptor Imaging (GLP1-EX-GELO)

Primary Purpose

Diabetes Mellitus, Non-Insulin-Dependent, Diabetes Mellitus

Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Gelofusine
111In-exendin 4 SPECT/CT
Placebo
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Diabetes Mellitus, Non-Insulin-Dependent focused on measuring SPECT, radiopeptides, gelofusine, Beta cell

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • >= 18 years
  • <= 60 years
  • Normal renal function
  • Normal glucose regulation
  • BMI 17>30

Exclusion Criteria:

  • Use of any medication affecting renal function
  • Known hypersensitivity to one of the substances used
  • Hypertension
  • Oedema
  • Hypervolaemia
  • Heart failure
  • Pregnancy or the wish to become pregnant within 3 months after participation of the study.
  • Lactation
  • History of anaphylaxis
  • Liver disease defined as aspartate aminotransferase or alanine aminotransferase level more than 3 times the upper limit of normal range (45U/L)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    gelofusine and 111In-exendin 4 SPECT/CT

    saline and 111In-exendin 4 SPECT/CT

    Arm Description

    subjects will receive a gelofusine injection before the injection of the radiopharmaceutical (111In-exendin 4)

    As a control, subjects will receive an injection of saline before the injection of the radiopharmaceutical (111In-exendin 4)

    Outcomes

    Primary Outcome Measures

    Renal uptake as measured by uptake of 111In-exendin-4 on SPECT images and without co-infusion of Gelofusine.

    Secondary Outcome Measures

    Pancreas uptake as measured by uptake of 111In-exendin-4 on SPECT images

    Full Information

    First Posted
    March 3, 2015
    Last Updated
    May 29, 2017
    Sponsor
    Radboud University Medical Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02541734
    Brief Title
    Effect of Gelofusine on GLP1-receptor Imaging
    Acronym
    GLP1-EX-GELO
    Official Title
    Effect of Gelofusine on 111In-DTPA-AHX-Lys40-Exendin 4 Uptake in the Kidney
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    August 2015 (undefined)
    Primary Completion Date
    May 2017 (Actual)
    Study Completion Date
    May 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Radboud University Medical Center

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The highly promising and innovative tracer on 111In-DTPA-AHX-Lys40-Exendin 4 has been applied to determine beta cell mass in healthy volunteers and patients with type 1 diabetes. However, the high retention of the tracer in the kidneys was leading to a kidney/pancreas uptake ratio of 41±23. This high renal uptake is complicating absolute BCM quantification by SPECT imaging. In order to reduce the kidney/pancreas uptake ratio, investigators propose a co-infusion with the plasma expander Gelofusine since it has been shown in several pre-clinical and clinical studies that Gelofusine can reduce the renal retention of several other, closely related tracers. When investigators are able to reduce the kidney/pancreas uptake ratio, these findings will improve the interpretation of clinical quantitative SPECT, having important implications for therapeutic decision making for patients with diabetes, insulinomas or congenital hyperinsulinism, and may also have a major impact on our understanding of the pathophysiology of these diseases.
    Detailed Description
    Beta-cell imaging in vivo Reliable, sensitive and specific non-invasive methods for comprehensive structural and functional characterization of living pancreatic beta-cells in vivo (and in vitro) would not only enhance our understanding of the pathophysiology of various diseases, but also enable longitudinal in vivo assessment of beta cell mass (BCM) and distribution in patients with e.g. diabetes (including patients who received beta cell replacement therapy). Additionally, it can help in diagnosing insulinomas and congenital hyperinsulinism and when coupled to other biomarkers it could aid patient stratification and enable patient-specific optimized treatment strategies. Inhibiting the reabsorption of radiolabelled peptides It has been shown, both in vitro and in vivo, that the kidney uptake of radiolabelled peptides can be reduced by co-infusion of agents that inhibit the reabsorption of these peptides. One of these agents is succinylated gelatin (Gelofusine), a plasma expander that consists of a mixture of collagen-derived peptides. Previous clinical observations have shown that Gelofusine infusion results in tubular proteinuria of both albumin and β2-microglobulin. Although the exact mechanism for this proteinuria is not completely understood, the megalin receptor system is most likely involved. Based on pre-clinical studies in mice and rats, it has been known that kidney uptake is significantly reduced for various tracers when co-infused with Gelofusine, like 111In-Octreotide 111In-Minigastrin, 68Ga-exendin-4 and 111In-DTPA-AHX-Lys40-Exendin 4. Additionally, it was shown that Gelofusine also reduces the renal retention of 111In- Octreotide by 45% in humans. In the current study, investigators will determine whether Gelofusine has also an effect on kidney retention of 111In-DTPA-AHX-Lys40-Exendin 4 in humans.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Diabetes Mellitus, Non-Insulin-Dependent, Diabetes Mellitus
    Keywords
    SPECT, radiopeptides, gelofusine, Beta cell

    7. Study Design

    Primary Purpose
    Basic Science
    Study Phase
    Phase 1, Phase 2
    Interventional Study Model
    Crossover Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    12 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    gelofusine and 111In-exendin 4 SPECT/CT
    Arm Type
    Experimental
    Arm Description
    subjects will receive a gelofusine injection before the injection of the radiopharmaceutical (111In-exendin 4)
    Arm Title
    saline and 111In-exendin 4 SPECT/CT
    Arm Type
    Placebo Comparator
    Arm Description
    As a control, subjects will receive an injection of saline before the injection of the radiopharmaceutical (111In-exendin 4)
    Intervention Type
    Drug
    Intervention Name(s)
    Gelofusine
    Intervention Description
    Infusion of gelofusine
    Intervention Type
    Radiation
    Intervention Name(s)
    111In-exendin 4 SPECT/CT
    Intervention Description
    111In-exendin 4 SPECT/CT
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Primary Outcome Measure Information:
    Title
    Renal uptake as measured by uptake of 111In-exendin-4 on SPECT images and without co-infusion of Gelofusine.
    Time Frame
    up to 8 months
    Secondary Outcome Measure Information:
    Title
    Pancreas uptake as measured by uptake of 111In-exendin-4 on SPECT images
    Time Frame
    up to 8 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: >= 18 years <= 60 years Normal renal function Normal glucose regulation BMI 17>30 Exclusion Criteria: Use of any medication affecting renal function Known hypersensitivity to one of the substances used Hypertension Oedema Hypervolaemia Heart failure Pregnancy or the wish to become pregnant within 3 months after participation of the study. Lactation History of anaphylaxis Liver disease defined as aspartate aminotransferase or alanine aminotransferase level more than 3 times the upper limit of normal range (45U/L)
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Martin Gotthardt, Prof Dr
    Organizational Affiliation
    Radboud University Medical Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Effect of Gelofusine on GLP1-receptor Imaging

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