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ADI-PEG20, Obesity and Prediabetes

Primary Purpose

Obesity, PreDiabetes

Status
Not yet recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
ADI-PEG20
Placebo
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity

Eligibility Criteria

18 Years - 22 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: age: ≥18 and ≤22 years; BMI 25.0 - 44.9 kg/m2; Prediabetes, defined as fasting plasma glucose of ≥100 mg/dL, or HbA1C ≥5.7%, or HOMA-IR ≥2.5. Exclusion Criteria: HbA1C ≥6.5%; Intolerance or allergies to ingredients in ADI-PEG20 or placebo; Taking dietary supplements or medications known to affect our study outcomes; Evidence of significant organ system dysfunction or diseases, Metallic implants, which would preclude MRI

Sites / Locations

  • Washington University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

ADI-PEG20

Placebo

Arm Description

ADI-PEG20 (ADI-PEG20 is arginine deiminase (ADI) conjugated to polyethylene glycol (PEG) of 20,000 molecular weight) will be weekly intramuscularly at a dose of 18 mg/m2 body surface area/week for 8-week.

Will be weekly intramuscularly for 8-week

Outcomes

Primary Outcome Measures

Change in insulin sensitivity
Insulin sensitivity will be assessed by using the hyperinsulinemic-euglycemic clamp procedure

Secondary Outcome Measures

Change in oral glucose tolerance
Oral glucose tolerance will be assessed by measuring plasma glucose concentrations before and after ingesting 75 grams glucose
Change in oral glucose tolerance
Oral glucose tolerance will be assessed by measuring plasma glucose concentrations before and after ingesting 75 grams glucose
Change in β-cell function
β-cell function will be assessed from a modified oral glucose tolerance test
Change in β-cell function
β-cell function will be assessed from a modified oral glucose tolerance test
Change in resting energy expenditure
Resting energy expenditure (in kcal/min) will be assessed by using indirect calorimetry
Change in muscle mitochondrial respiration
Muscle mitochondrial respiration (in pmol O2/mg tissue) will be assessed by using high resolution respirometry, conducted on permeabilized muscle fibers obtained by muscle biopsy.
Change in intrahepatic triglyceride content
Intrahepatic triglyceride content will be assessed by magnetic resonance imagining (MRI)

Full Information

First Posted
November 11, 2022
Last Updated
April 24, 2023
Sponsor
Washington University School of Medicine
Collaborators
Children's Discovery Institute, Polaris Pharmaceuticals, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT05829239
Brief Title
ADI-PEG20, Obesity and Prediabetes
Official Title
A Randomized Trial Using ADI-PEG20 to Improve Insulin- and Energy Homeostasis in Adolescents With Obesity
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 2023 (Anticipated)
Primary Completion Date
June 2025 (Anticipated)
Study Completion Date
September 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine
Collaborators
Children's Discovery Institute, Polaris Pharmaceuticals, Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Th purpose of this study is to determine whether ADI-PEG20 (PEGylated arginine deiminase), an arginine catabolizing enzyme preparation, improves insulin sensitivity, mitochondrial respiration, and energy utilization in adolescents with prediabetes.
Detailed Description
Obesity, insulin resistance, and their complications are major causes of morbidity and mortality in children, adolescents, and adults. Although caloric restriction is an effective treatment, intensive lifestyle changes are rarely durable. The investigators and others have shown that: (i.) fasting incites arginine catabolism, and forced arginine catabolism recapitulates several therapeutic effects of fasting, (ii.) exogenous, forced arginine catabolism improves metabolic health, and (iii.) ADI-PEG20 (PEGylated arginine deiminase) is an arginine catabolizing enzyme preparation that improves insulin sensitivity, mitochondrial respiration, and energy utilization in obese mice. The study will determine whether ADI-PEG20 also exerts beneficial effects on metabolic healthy in people. The investigators will perform a 12-week, randomized, double-blind, placebo-controlled trial in boys and girls with pre-diabetes to evaluate the efficacy of ADI-PEG20 treatment on: 1) body composition; 2) resting energy expenditure; 3) multi-organ insulin sensitivity; 3) β-cell function; and 4) muscle mitochondrial function.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, PreDiabetes

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Single-center, randomized, double-blind, placebo-controlled study
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
48 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ADI-PEG20
Arm Type
Experimental
Arm Description
ADI-PEG20 (ADI-PEG20 is arginine deiminase (ADI) conjugated to polyethylene glycol (PEG) of 20,000 molecular weight) will be weekly intramuscularly at a dose of 18 mg/m2 body surface area/week for 8-week.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Will be weekly intramuscularly for 8-week
Intervention Type
Biological
Intervention Name(s)
ADI-PEG20
Intervention Description
Intramuscular injection weekly for 8 weeks
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Intramuscular injection weekly for 8 weeks
Primary Outcome Measure Information:
Title
Change in insulin sensitivity
Description
Insulin sensitivity will be assessed by using the hyperinsulinemic-euglycemic clamp procedure
Time Frame
Baseline and 8 weeks of ADI-PEG20 or placebo
Secondary Outcome Measure Information:
Title
Change in oral glucose tolerance
Description
Oral glucose tolerance will be assessed by measuring plasma glucose concentrations before and after ingesting 75 grams glucose
Time Frame
Baseline and 4 weeks of ADI-PEG20 or placebo
Title
Change in oral glucose tolerance
Description
Oral glucose tolerance will be assessed by measuring plasma glucose concentrations before and after ingesting 75 grams glucose
Time Frame
Baseline and 8 weeks of ADI-PEG20 or placebo
Title
Change in β-cell function
Description
β-cell function will be assessed from a modified oral glucose tolerance test
Time Frame
Baseline and 4 weeks of ADI-PEG20 or placebo
Title
Change in β-cell function
Description
β-cell function will be assessed from a modified oral glucose tolerance test
Time Frame
Baseline and 8 weeks of ADI-PEG20 or placebo
Title
Change in resting energy expenditure
Description
Resting energy expenditure (in kcal/min) will be assessed by using indirect calorimetry
Time Frame
Baseline and 8 weeks of ADI-PEG20 or placebo
Title
Change in muscle mitochondrial respiration
Description
Muscle mitochondrial respiration (in pmol O2/mg tissue) will be assessed by using high resolution respirometry, conducted on permeabilized muscle fibers obtained by muscle biopsy.
Time Frame
Baseline and 8 weeks of ADI-PEG20 or placebo
Title
Change in intrahepatic triglyceride content
Description
Intrahepatic triglyceride content will be assessed by magnetic resonance imagining (MRI)
Time Frame
Baseline and 8 weeks of ADI-PEG20 or placebo
Other Pre-specified Outcome Measures:
Title
Change in the transcriptome in muscle
Description
The transcriptome will be evaluated by using RNA sequencing techniques
Time Frame
Baseline and 8 weeks of ADI-PEG20 or placebo
Title
Change in the transcriptome in adipose tissue
Description
The transcriptome will be evaluated by using RNA sequencing techniques
Time Frame
Baseline and 8 weeks of ADI-PEG20 or placebo

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
22 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age: ≥18 and ≤22 years; BMI 25.0 - 44.9 kg/m2; Prediabetes, defined as fasting plasma glucose of ≥100 mg/dL, or HbA1C ≥5.7%, or HOMA-IR ≥2.5. Exclusion Criteria: HbA1C ≥6.5%; Intolerance or allergies to ingredients in ADI-PEG20 or placebo; Taking dietary supplements or medications known to affect our study outcomes; Evidence of significant organ system dysfunction or diseases, Metallic implants, which would preclude MRI
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nikki Plassmeyer, MA, RDN, LD
Phone
314-362-0590
Email
nikkip@wustl.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Samuel Klein, MD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington University School of Medicine
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nikki Plassmeyer, MA, RDN, LD
Phone
314-362-0590
Email
nikkip@wustl.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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ADI-PEG20, Obesity and Prediabetes

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