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Fr1da Insulin Intervention

This study is currently recruiting participants.
See Contacts and Locations
Verified November 2016 by Technische Universität München
Sponsor:
Collaborators:
Technische Universität Dresden
Ludwig-Maximilians - University of Munich
Helmholtz Zentrum München
The Leona M. and Harry B. Helmsley Charitable Trust
Information provided by (Responsible Party):
Technische Universität München
ClinicalTrials.gov Identifier:
NCT02620072
First received: November 29, 2015
Last updated: November 9, 2016
Last verified: November 2016
  Purpose
Type 1 diabetes (T1D) results from an autoimmune destruction of the insulin-producing beta cells. The process of autoimmune destruction is identified by circulating islet autoantibodies to beta cell antigens, and is mediated by a lack of immunological self-tolerance. Self-tolerance is achieved by T cell exposure to antigen in the thymus or periphery in a manner that deletes autoreactive effector T cells or induces regulatory T cells. Immunological tolerance can be achieved by administration of antigen under appropriate conditions. Evidence is now emerging in humans that these approaches may be effective in chronic inflammatory diseases such as multiple sclerosis and allergy. Administration of oral insulin in multiple islet autoantibody-positive children offers the potential for inducing immunological tolerance to beta cells and thereby protect against further development progression to type 1 diabetes.

Condition Intervention Phase
Diabetes Mellitus, Type 1 Drug: Oral Insulin Other: Placebo Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double Blind (Participant, Care Provider, Investigator)
Primary Purpose: Prevention
Official Title: Mechanistic Study Using Oral Insulin for Immune Efficacy in Secondary Prevention of Type 1 Diabetes

Resource links provided by NLM:


Further study details as provided by Technische Universität München:

Primary Outcome Measures:
  • (1) Immune response: The activation of a protective immune response against insulin (immune responder status) and (2) Immune efficacy: rate of progression to dysglycemia in immune responders vs. non-responders [ Time Frame: (1) change from baseline in CD4+ T cell response measured as a stimulation index at 12 months after the end of treatment and (2) comparison of the rate of progression to dysglycemia at end of FU (12 mon. after treatment in last enrolled partic.) ]

    Study includes two co-primary outcomes:

    Analysis of co-primary outcomes is hierarchical. Order of hierarchy: 1st: immune response. If significant, analysis will proceed to 2nd: immune efficacy.

    (1) Immune response: children will be categorized as having or not having response to insulin during treatment. Outcome is positive when a child has one or more of the following three responses at one or more times points during follow-up:

    1. a pos. salivary IgA-IAA (at 3-, 6-, 12 months)
    2. a >2-fold increase in CD4+ T cell response to insulin (at 3-, 9-, 12 months)
    3. a >2-fold increase in number of circulating Insulin-tetramer pos. CD4+CD25+FOXP3+ T cells (at 6 months).

    Number between placebo- and study drug responder will be compared.

    (2) Immune efficacy: comparing progression rates in children with without change in immune response to insulin, regardless of treatment group. Comparison will be made using the Cox regression at the 0.05 level, two-sided.



Secondary Outcome Measures:
  • Gene expression of single cells. [ Time Frame: Gene expression profile measurement on insulin-responsive cells at 12 month visit ]
    The FOXP3 signature/IFNG signature ratio of the insulin responsive cells will be compared between the placebo and study drug treated children. In addition the gene expression of all analyzed genes will be compared between the placebo and study drug treated groups using tSNE.

  • The change from baseline in IgG-binding to insulin [ Time Frame: change from baseline to 3 months, 6, months, and 12 months ]
    The change in IgG-binding to insulin will be measured by radio-binding assay. It will be compared between placebo and study drug treated children at the 3 months, 6 months, and 12 months time points using ANOVA and normalized data.

  • The change from baseline in IgG4-binding to insulin [ Time Frame: change from baseline to 3 months, 6, months, and 12 months ]
    The change in IgG4-binding to insulin will be measured by radio-binding assay. It will be compared between placebo and study drug treated children at the 3 months, 6 months, and 12 months time points using ANOVA and normalized data.

  • Number of circulating Insulin-tetramer positive T cells [ Time Frame: comparison at 9 month visit ]
    The number of circulating Insulin-tetramer positive CD4+CD25+FOXP3+ T cells (measured at 9 months) will be compared between placebo and study drug treated children using ANOVA.

  • Progression to diabetes [ Time Frame: Measured at baseline (visit 1) and at each subsequent visit of the treatment phase (visits 2, 3, 4, 5) and observational follow-up of 24 to 54 months after the one year treatment (visits 6, 7, 8, 9, 10, 11, 12, 13, 14) ]
    Progression to diabetes will be monitored and compared between placebo and study drug treated children using the Cox regression at the 0.05 level, two-sided. With 220 children randomized over a 30 month period, and a study duration of 66 month, the study will have 86% power to detect a 50% reduction in the rate of progression to diabetes at a two-sided alpha of 0.05.


Other Outcome Measures:
  • Hypoglycemia [ Time Frame: Measured at baseline (visit 1) and at subsequent change in dose (visits 2). ]
    Metabolic changes within two hours after receiving study drug. This will be performed at the first administration of oral insulin or placebo at each new dose (visit 1 and visit 2). At these visits, blood glucose concentrations will be measured at 0 minutes, 30 minutes, 60 minutes, and 120 minutes after receiving study drug to determine whether the treatment induces hypoglycaemia which is defined as <50 mg/dl (<2.8 mmol/L).

  • Adverse events [ Time Frame: Duration of participation from study visit 1 until the end of the study (min. 36 months, max. 66 months) or drop out ]
    Adverse events are reported throughout the period of participation of each participant. Analysis will compare the number and frequency of adverse events during treatment with study drug (total and during each dose period) to the number and frequency of adverse events in the placebo treated children.


Estimated Enrollment: 220
Study Start Date: December 2015
Estimated Study Completion Date: June 2021
Estimated Primary Completion Date: June 2021 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: oral insulin capsule (dose escalation using 2 dose strengths)
Dose 1 is 7.5 mg rH-insulin crystals; dose 2 is 67.5 mg rH-insulin crystals. Insulin crystals are formulated together with filling substance (microcrystalline cellulose to a total weight of 200 mg) contained in hard gelatine capsules given orally.
Drug: Oral Insulin
Total of 12 months treatment; dose escalation scheme: daily treatment with 7.5 mg or placebo for 3 months; increasing to daily treatment with 67.5 mg or placebo for the following 9 months of the treatment period. Follow-up will continue for 24 months after the last administration of treatment.
Placebo Comparator: Placebo capsule
Daily administration of placebo capsules containing filling substance (microcrystalline cellulose).
Other: Placebo
Total of 12 months intervention period; daily administration of insulin or placebo capsules containing filling substance (microcrystalline cellulose). Follow-up will continue for 24 months after the last administration of treatment.

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   2 Years to 12 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Written informed consent signed by either parent(s) or legal guardian(s).
  2. Children aged 2 years to 12 years.
  3. Positive for at least two islet autoantibodies out of autoantibodies to glutamic acid decarboxylase (GAD65), to insulin (IAA), autoantibodies to IA-2 (IA2A), or autoantibodies to zink transporter 8 (ZnT8A) (time between screening sample collection and randomization must not exceed 90 days).
  4. Normoglycemia assessed by oral glucose tolerance test (OGTT).
  5. Participation in an observational study that regularly monitors diabetes development

Exclusion Criteria:

Participants meeting any of the following criteria will NOT be eligible for inclusion into the study:

  1. dysglycaemia or overt hyperglycemia (diabetes)
  2. Concomitant disease or treatment that may interfere with assessment or cause immunosuppression, as judged by the investigators.
  3. Current participation in another intervention trial.
  4. Any condition that could be associated with poor compliance.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT02620072

Contacts
Contact: Anette-G. Ziegler, Prof. Dr. +49 89 3187 ext 2896 anette-g.ziegler@helmholtz-muenchen.de

Locations
Germany
Forschergruppe Diabetes, Klinikum rechts der Isar, Technische Universität München, Lehrstuhl für Diabetes und Gestationsdiabetes, der Technischen Universität München Recruiting
München, Deutschland (DEU), Germany, 80804
Contact: Anette-G. Ziegler, Prof. Dr., MD    +49 (0)800 464 ext 8835    diabetes.frueherkennung@helmholtz-muenchen.de   
Sponsors and Collaborators
Technische Universität München
Technische Universität Dresden
Ludwig-Maximilians - University of Munich
Helmholtz Zentrum München
The Leona M. and Harry B. Helmsley Charitable Trust
Investigators
Principal Investigator: Anette-G. Ziegler, Prof. Dr., MD Forschergruppe Diabetes, Klinikum rechts der Isar, Technische Universität München
Study Chair: Ezio Bonifacio, Prof. Dr., PhD Paul Langerhans Institute Dresden (PLID) of the Helmholtz Zentrum München at the Universitätsklinikum Carl Gustav Carus, Technische Universität Dresden
Principal Investigator: Peter Achenbach, PD. Dr., MD Forschergruppe Diabetes, Klinikum rechts der Isar, Technische Universität München
Principal Investigator: Katharina Warncke, Dr., MD Forschergruppe Diabetes, Klinikum rechts der Isar, Techn. Universität München and Kinderklinik München Schwabing, Klinik u. Poliklinik f. Kinder- und Jugendmedizin, Klinikum Schwabing, StKM GmbH und Klinikum rechts der Isar der Techn. Universität München
Study Chair: Christiane Winkler, Dr., PhD Forschergruppe Diabetes, Klinikum rechts der Isar, Technische Universität München
  More Information

Additional Information:
Responsible Party: Technische Universität München
ClinicalTrials.gov Identifier: NCT02620072     History of Changes
Other Study ID Numbers: 808040019
Study First Received: November 29, 2015
Last Updated: November 9, 2016

Keywords provided by Technische Universität München:
Type 1 diabetes
T1D
diabetes mellitus
oral insulin
oral tolerance
autoantigen
self tolerance
prevention
at risk for developing type 1 diabetes
juvenile diabetes
dysglycemia

Additional relevant MeSH terms:
Diabetes Mellitus
Diabetes Mellitus, Type 1
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Autoimmune Diseases
Immune System Diseases
Insulin, Globin Zinc
Insulin
Hypoglycemic Agents
Physiological Effects of Drugs

ClinicalTrials.gov processed this record on July 21, 2017