AbATE Follow-Up Study

NCT ID: NCT02067923

Last Updated: 2018-01-17

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 44 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2014-02-28
• Study Completion Date: 2016-11-17

Brief Summary

This study proposes to conduct a non-interventional, multi-center trial that will look at C-peptide results from one or two Mixed Meal Tolerance Tests (MMTT) in participants who received anti-CD3 treatment or placebo on the Abate ITN027AI trial. Anti-CD3 monoclonal antibody is a humanized antibody that is commonly used to prevent organ rejection. It was give in order to determine whether anti-CD3 mAb treatment can halt the progression of newly diagnosed type 1 diabetes.

The overall hypothesis of this study is there will be less change in c-peptide levels of the previously treated group versus the control group.

Detailed Description

We propose to conduct a non-interventional multi-center trial that will look at C-peptide results from one or two Mixed Meal Tolerance Tests (MMTT) in participants who received anti-CD3 treatment or placebo on the Abate ITN027AI trial. The first few subjects went on the trial late in 2005 and the last subjects were enrolled in 2009.The mixed meal tolerance tests will coincide with approximately 4 years and 6 years post ITN027AI study completion for each participant. Those participants, who completed the ITN027AI study in 2007 and 2008, will only have a single MMTT.

We plan to enroll approximately 77 subjects at 5 sites who were previously active with ITN027AI.. Both the drug treated and the control group participants will be invited to participate. Along with Yale University these sites include, the University of California-San Francisco, University of Colorado-Barbara Davis, Benaroya Research Institute, and Pacific Northwest Research Institute -University of Washington. The investigators of each of these sites will be asked to contact their patients who were originally on the ITN027AI study.

Subjects will be contacted via email or phone to see if they would be interested in participating on this Abate follow-up study. Eligible participants will come to the Yale University Church St. Research Unit or other participating ITN study site for either 1 or 2 mixed meal tolerance tests to determine their current c-peptide status. The available sites for participants to go to include: Yale University, University of California-San Francisco, University of Colorado-Barbara Davis Center, Benaroya Research Institute and Pacific Northwest-University of Washington.

This first visit will consist of the following: an explanation of the study, an assessment of inclusion/exclusion criteria and documentation of informed consent. If the subject meets the inclusion/exclusion criteria, a complete medical history will be obtained, physical examination including vital signs, urine pregnancy test if a female of childbearing potential and an assessment of concomitant medications. The subject will then have a Mixed Meal Tolerance Tests (MMTT) with a possible 2nd MMTT with C-Peptide and glucose measurements a year later based on how long it has been since they were on the ITN027AI Study.The subject will also have a 4 hour urine collection for C-peptide and creatinine during this MMTT. If a repeat MMTT is done a year later then another 4 hour urine sample during the MMTT will be collected for C-peptide and Creatinine measurement.

Conditions

Diabetes Mellitus, Type 1

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Anti-CD3 mAb Plus Diabetes Standard of Care Group

This group of individuals received treatment in the original AbATE study.

No interventions assigned to this group

Diabetes Standard of Care Group

During the original AbATE study these individuals received standard care.

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Prior participation on either the treatment or the control arm of the Abate ITN027AI trial
• Signed Informed Consent

Exclusion Criteria

• Inability or unwillingness to give informed consent
• Participation in an investigational treatment trial within the last 6 weeks before enrollment
• Ongoing major systemic illness.
• Clinically active serious infections.
• Any medical condition that in the opinion of the investigator would interfere with safe completion of the trial.
• Positive pregnancy test in menstruating women
• Actively breast feeding

• Minimum Eligible Age: 10 Years
• Maximum Eligible Age: 37 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Yale University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Kevan Herold, MD

Role: PRINCIPAL_INVESTIGATOR

Yale University

Locations

Church Street Research Unit

New Haven, Connecticut, United States

Countries

United States

References

Perdigoto AL, Preston-Hurlburt P, Clark P, Long SA, Linsley PS, Harris KM, Gitelman SE, Greenbaum CJ, Gottlieb PA, Hagopian W, Woodwyk A, Dziura J, Herold KC; Immune Tolerance Network. Treatment of type 1 diabetes with teplizumab: clinical and immunological follow-up after 7 years from diagnosis. Diabetologia. 2019 Apr;62(4):655-664. doi: 10.1007/s00125-018-4786-9. Epub 2018 Dec 19.

Reference Type: DERIVED

PMID: 30569273 (View on PubMed)

Other Identifiers

1310012954

Identifier Type: -

Identifier Source: org_study_id