Diabetes Virus Detection Project, Intervention With GAD-alum (DiViD)
Primary Purpose
Diabetes, Type I, Enterovirus Infections, Autoimmunity
Status
Terminated
Phase
Phase 2
Locations
Norway
Study Type
Interventional
Intervention
GAD-alum
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Diabetes, Type I focused on measuring insulin
Eligibility Criteria
Inclusion Criteria:
- Newly diagnosed classical type-1 diabetes
- Positive GAD antibodies
- Fasting C-peptide >0.1 mmol/l
- Insulin dosage >0.1 U/kg Bodyweight/day
Exclusion Criteria:
- Pregnancy
- Weaning
- Other chronic diseases than diabetes
- Any regular medication except oral contraceptives
- Psychiatric disturbances
Sites / Locations
- Endokrinologisk poliklinikk, Oslo Universitetssykehus Aker
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
GAD-alum
Placebo
Arm Description
GAD-alum administered at 0 and 1 months after inclusion
Outcomes
Primary Outcome Measures
Intensity of insulitis in proportion to living, insulin-staining beta cells in pancreatic biopsies
Prevalence of virus infected islets in pancreatic biopsies
Intensity of insulitis in proportion to living, insulin-staining beta cells in pancreatic biopsies
Prevalence of virus infected islets in pancreatic biopsies
Secondary Outcome Measures
Residual insulin secretion (C-peptide) measured by Mixed Meal Tolerance Test
Will be measured at 0, 1, 3, 9, 18, 24 and 36 months after diagnosis, but time frame is at 36 months
Insulin dosage/kilo bodyweight/24 hours
Will be calculated at 0, 1, 3, 9, 18, 24 and 36 months after diagnosis, but time frame is 36 months after diagnosis
Glycosylated hemoglobin A1 (HbA1c)
Will be measrured at 0, 1, 3, 9, 18, 24 and 36 months after diagnosis, but time frame is at 36 months. To investigate wether an eventual better endogenous insulin production gives better metabolic control, estimated by lower HbAic
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01129232
Brief Title
Diabetes Virus Detection Project, Intervention With GAD-alum
Acronym
DiViD
Official Title
A Phase II-study (Therapeutic Exploratory) of GAD-alum in Newly Diagnosed Type-1 Diabetic Patients, With Focus One the Presence of Viruses at the Time of Diagnosis
Study Type
Interventional
2. Study Status
Record Verification Date
May 2018
Overall Recruitment Status
Terminated
Why Stopped
Complications to procedure
Study Start Date
January 2011 (undefined)
Primary Completion Date
January 2013 (Actual)
Study Completion Date
January 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purposes of this study are to test whether GAD vaccination can stop the progression of newly diagnosed type 1 diabetes, to describe the related immunological processes (insulitis) in pancreas and small intestines evolving the mechanism of the effect of GAD vaccination and finally try to detect viruses and virus receptors directly in the insulin producing beta cells of the pancreas in patients with newly diagnosed type-1 diabetes mellitus (T1D).
Detailed Description
The aetiology of type 1 diabetes is unknown. Both genetic and environmental factors seem to be important for the destruction of insulin producing beta cells in the pancreas. Increasing indirect evidences exist that picornaviruses may either directly or indirectly through autoimmune processes destroy beta cells. New sensitive assays have been developed to detect these viruses and to study the immunological processes, especially T-cell function. Microsurgical technology has been refined, now making pancreatic biopsies a safe procedure. This study focuses on advanced in depth studies of immunology and virology in pancreatic tissue and small intestine at an early stage of disease.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes, Type I, Enterovirus Infections, Autoimmunity
Keywords
insulin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
6 (Actual)
8. Arms, Groups, and Interventions
Arm Title
GAD-alum
Arm Type
Experimental
Arm Description
GAD-alum administered at 0 and 1 months after inclusion
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
GAD-alum
Other Intervention Name(s)
Diamyd
Intervention Description
20 µg of GAD-alum injected sc after the biopsy, and repeated after one month
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo injected after the biopsy and repeated after one month (similar to the GAD-alum-arm)
Primary Outcome Measure Information:
Title
Intensity of insulitis in proportion to living, insulin-staining beta cells in pancreatic biopsies
Time Frame
18 months after inclusion
Title
Prevalence of virus infected islets in pancreatic biopsies
Time Frame
18 months after inclusion
Title
Intensity of insulitis in proportion to living, insulin-staining beta cells in pancreatic biopsies
Time Frame
2 weeks after inclusion
Title
Prevalence of virus infected islets in pancreatic biopsies
Time Frame
2 weeks after inclusion
Secondary Outcome Measure Information:
Title
Residual insulin secretion (C-peptide) measured by Mixed Meal Tolerance Test
Description
Will be measured at 0, 1, 3, 9, 18, 24 and 36 months after diagnosis, but time frame is at 36 months
Time Frame
36 months after diagnosis
Title
Insulin dosage/kilo bodyweight/24 hours
Description
Will be calculated at 0, 1, 3, 9, 18, 24 and 36 months after diagnosis, but time frame is 36 months after diagnosis
Time Frame
36 months after diagnosis
Title
Glycosylated hemoglobin A1 (HbA1c)
Description
Will be measrured at 0, 1, 3, 9, 18, 24 and 36 months after diagnosis, but time frame is at 36 months. To investigate wether an eventual better endogenous insulin production gives better metabolic control, estimated by lower HbAic
Time Frame
36 months after diagnosis
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Newly diagnosed classical type-1 diabetes
Positive GAD antibodies
Fasting C-peptide >0.1 mmol/l
Insulin dosage >0.1 U/kg Bodyweight/day
Exclusion Criteria:
Pregnancy
Weaning
Other chronic diseases than diabetes
Any regular medication except oral contraceptives
Psychiatric disturbances
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Knut Dahl-Jorgensen, Prof
Organizational Affiliation
Oslo University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Endokrinologisk poliklinikk, Oslo Universitetssykehus Aker
City
Oslo
ZIP/Postal Code
0514
Country
Norway
12. IPD Sharing Statement
Learn more about this trial
Diabetes Virus Detection Project, Intervention With GAD-alum
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