An Innovative Approach Towards Understanding and Arresting Type 1 Diabetes (INNODIA) (INNODIA)
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|ClinicalTrials.gov Identifier: NCT03936634|
Recruitment Status : Recruiting
First Posted : May 3, 2019
Last Update Posted : May 10, 2019
INNODIA is a global consortium linking 26 academic institutions, 4 industrial partners, a small to medium enterprise (SME), and 2 patient organisations, bringing their knowledge and experience together with one common goal: "To fight type 1 diabetes". (www.innodia.eu).
The project, approved in November 2015 and launched in January 2016, runs under the framework of the Innovative Medicines Initiative - Joint Undertaking (https://www.imi.europa.eu/projects-results/project-factsheets/innodia) with a dedicated governance structure ensuring close interaction, communication and adherence to the objectives and deliverables of the consortium.
The overall aim of INNODIA is to advance in a decisive way how to predict, stage, evaluate and prevent the onset and progression of type 1 diabetes (T1D). For this, INNODIA has established a comprehensive and interdisciplinary network of clinical and basic scientists, who are leading experts in the field of T1D research in Europe, with complementary expertise from the areas of immunology, Beta-cell biology, biomarker research and T1D therapy, joining forces in a coordinated fashion with industry partners and two foundations, as well as with all major stakeholders in the process, including regulatory bodies and patients with T1D and their families.
One of the objectives of INNODIA is to develop a new European clinical research network with standardized protocol based on repeated measures of C-peptide (including home measurements) and comprehensive collection of appropriate biological samples for 'omics', immune, viral and microbiome studies in new onset T1D patients and high-risk auto-antibody positive subjects. A protocol for the harmonization of sample collections in newly diagnosed type 1 diabetic patients and first degree relatives of patients with type 1 diabetes was developed following extensive preliminary work involving partners from across all specialities. Core laboratories with experience in their respective field were set up for analysis of auto-antibodies, fresh immune cells, handling of frozen immune cells, C-peptide measures. A series of standard operating procedures for sample collections and analysis were agreed. Sample tracking between clinical centres and central laboratories was included into a purposely designed electronic case report form (eCRF) into which all clinical and laboratory data collected are captured.
|Condition or disease|
|Type 1 Diabetes Mellitus|
This is a longitudinal observational study of the relationship between measures of β-cell function, genotype, immunological phenotype and potential environmental factors over time, in individuals with new onset T1D or first degree relatives at higher risk for T1D due to the presence of auto-antibodies.
It is a multicentre international study involving clinical centres across Europe which is unique in the following ways:
- The first such collaboration in Europe
- Novel evaluation of C-peptide/β-cell function using both home dried blood spots and regular hospital mixed meal tolerance tests or oral glucose tolerance tests
- Identical study procedures across all clinical centres
- Centralised analysis/storage of clinically relevant samples
- The creation of a living 'Biobank' whereby participants can be recalled for study on the basis of specific genotype/phenotypes
- Linkage to innovative study of novel biomarkers to inform future interventional strategies
- A potential pipeline for future recruitment and consent to novel innovative interventional strategies
The study is divided into 2 arms:
In arm A, the investigators plan to recruit 1500 newly diagnosed T1D patients within 6 weeks from diagnosis. The last study visit will be planned 2 years from diagnosis or until the end of the study. Therefore, the duration of the study will be approximately 2 years consisting of 5 visits. At baseline, C-peptide and immunophenotyping are evaluated. Follow up consists of regular mixed meal tolerance test (MMTT) and providing blood, urine and stool samples for 'omics', immune, viral and microbiome studies. Home dried blood spots (DBS) pre and post a standardized meal will be collected monthly for the duration of the study.
These recruited participants will be included for further observational study, confirmation of potential biomarkers and will ultimately provide a pipeline for future recruitment to interventional studies.
In arm B, the investigators plan to screen approximately 3000 unaffected first degree family members across all centres during the first 3 years. The family members will be screened for 4 auto-antibodies (GAD65, IA-2A, IAA, ZnT8A).
Unaffected family members who are auto-antibody positive will be followed up for approximately 4 years consisting of visits every 6 months for the first 2 years and then every 12 months until the end of the study. Follow up will consist of regular oral glucose tolerance test (OGTT) and providing blood, urine and stool samples for 'omics', immune, viral and microbiome studies. Home dried blood spots (DBS) will be collected monthly for the duration of the study.
Unaffected participants who are auto-antibody negative will be sent annual questionnaires until the end of the study.
All study participants will be consented to a living 'Biobank' where we will be able to request participants to be recalled by genotype/phenotype for further studies involving blood, urine and stool samples.
|Study Type :||Observational [Patient Registry]|
|Estimated Enrollment :||4500 participants|
|Target Follow-Up Duration:||2 Years|
|Official Title:||An Innovative Approach Towards Understanding and Arresting Type 1 Diabetes (INNODIA)|
|Actual Study Start Date :||November 14, 2016|
|Estimated Primary Completion Date :||October 31, 2022|
|Estimated Study Completion Date :||October 31, 2022|
Newly Diagnosed (ND)
Recruited within 6 weeks of type 1 diabetes diagnosis. Age between 1 and <45 years
Unaffected Family members (UFM)
Participants who are not diabetic but have a first degree relative with type 1 diabetes diagnosed < 45 years of age.
Age between 1 and <45 years
- Arm A - Newly Diagnosed people with Type 1 diabetes [ Time Frame: 24 months ]Rate of decline in Beta cell function as assessed by mixed meal tolerance test and home dried blood spot C-peptide measures over the first 24 months from diagnosis of Type 1 diabetes.
- Arm B - Auto-antibody positive first degree family members [ Time Frame: 48 months ]Development of diabetes as defined by the American Diabetes Association in auto-antibody positive family members followed longitudinally.
- Arm A - Newly diagnosed patients with Type 1 diabetes [ Time Frame: 24 months ]Changes in HbA1c, insulin dose, autoantibody levels over the first 24 months from diagnosis.
- Arm A - Newly diagnosed patients with Type 1 diabetes - Systematic evaluation of biological samples [ Time Frame: 24 months ]Systematic evaluation of biological samples using multiple 'omics' approach to identify biomarkers which predict rate of deterioration in C-peptide measures
- Arm A - Newly diagnosed patients with Type 1 diabetes - Framework [ Time Frame: 24 months ]To develop a robust observational framework for future interventional studies.
- Arm B - Auto-antibody positive first degree family members - glucose tolerance [ Time Frame: 48 months ]Changes in glucose tolerance as determined by repeated oral glucose tolerance tests over the follow up period of 48 months
- Arm B - Auto-antibody positive first degree family members - Systematic evaluation of biological samples [ Time Frame: 48 months ]Systematic evaluation of biological samples, using multiple 'omics' approach, auto antibodies to identify biomarkers which predict rate of progression to diabetes.
- Arm B - Auto-antibody positive first degree family members - Framework [ Time Frame: 48 months ]Developing a robust framework for future interventional studies.
Biospecimen Retention: Samples With DNA
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03936634
|Contact: David B Dunger||+44 1223 firstname.lastname@example.org|
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|Study Chair:||Chantal Mathieu||Katholieke Universteit Leuven|