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Clinical trialNCT03751007CompletedPhase 1/PHASE2Interventional

A Study to Assess the Safety and Tolerability of Different Doses of AG019 Administered Alone or in Combination With Teplizumab in Participants With Recent-onset Diagnosed Type 1 Diabetes (T1D)

SponsorPrecigen Actobio T1D, LLCEnrollment45Diabetes type1
View the registry record on ClinicalTrials.gov

Summary

The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

  • Chantal Mathieu, MD

    University Hospital of Leuven, Clinical and Experimental Endocrinology

    Principal Investigator
  • Kevan Herold, MD

    Yale Center for Clinical Investigation; Yale University

    Principal Investigator

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

18 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Belgium
  • Uz Brussel

    Brussels, Belgium

  • Uz Antwerpen

    Edegem, Belgium

  • Uz Leuven

    Leuven, Belgium

United States
  • University of Alabama, Birmingham

    Birmingham, Alabama, United States

  • University of California, San Francisco

    San Francisco, California, United States

  • Coastal Metabolic Research Centre

    Ventura, California, United States

  • University of Colorado

    Aurora, Colorado, United States

  • Yale Center for Clinical Investigation

    New Haven, Connecticut, United States

  • University of Miami

    Miami, Florida, United States

  • University of South Florida

    Tampa, Florida, United States

  • Barry J Reiner, Md, Llc

    Baltimore, Maryland, United States

  • University of Minnesota Health

    Minneapolis, Minnesota, United States

  • University of Missouri-Kansas City School of Medicine

    Kansas City, Missouri, United States

  • Sanford Children'S Specialty Clinic

    Sioux Falls, South Dakota, United States

  • University Diabetes and Endocrine Consultants

    Chattanooga, Tennessee, United States

  • Texas Diabetes & Endocrinology, P.A.

    Austin, Texas, United States

  • Research Institute of Dallas

    Dallas, Texas, United States

  • Benaroya Research Institute

    Seattle, Washington, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
24 Oct 2018
Primary completion
13 Oct 2021
Completion
13 Oct 2021
Last update posted
1 Feb 2023
Registered enrollment
45
Registry id
NCT03751007

Cross-registrations

EU-CTR / CTIS (EudraCT)2017-002871-24

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.