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NCT04118153CompletedEarly phase 1

Early Markers of Disease and Response to Therapy

Source: ClinicalTrials.gov · Last updated 4 Jun 2024

Brief summary (registry, in English)

The purpose of this study is to identify early immune markers associated with response to treatment with abatacept in individuals with Type 1 diabetes (T1D). In this open label mechanistic study, participants who were recently diagnosed with T1D (males or females, ages 6-45 and \<7months from T1D diagnosis) will be treated with a short-course of abatacept (weekly subcutaneous injections for 3 months). Participants will undergo baseline and repeated mixed meal tolerance testing (MMTT) to assess disease progression and blood samples will be obtained at frequent intervals to measure changes in immune markers.

Status (registry)
Completed
Phase (registry)
Early phase 1
Study type
Interventional
Enrollment
60 (actual)
First submitted
2 Oct 2019
Start date
5 Mar 2021
Primary completion date
24 May 2024
Lead sponsor
Sandra Lord, MD
NCT number
NCT04118153

What you commit to

  • Study type: Interventional · Early phase 1
  • Participants enrolled: 60
  • From 5 Mar 2021 to the primary completion date, 24 May 2024
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Concurrent or recent (within the past 30 days of screening MMTT (visit -1)) use of non-insulin therapies aimed to control hyperglycemia
  • Receipt of live vaccine (MMR, intranasal influenza, varicella, rotatvirus) in 3 months before treatment

Other illness

  • Have an active infection at time of screening or baseline visit
  • Recent exposure, or possible or known active SARS-CoV-2 infection as defined by public health guidelines
  • Positive QuantiFERON or PPD TB test, history of tuberculosis, or active TB infection
  • Active infection with EBV or CMV, defined by real-time PCR
  • History of other clinically significant autoimmune disease needing chronic therapy with biologics or steroids with the exception of celiac disease and stable thyroid disease
  • Require use of other immunosuppressive agents for any other condition
  • Have serologic evidence of current or past HIV, Hepatitis B (positive for Hepatitis B core antibody or surface antigen), or Hepatitis C infection.
  • Have a history of malignancies

Lab values

  • Use of medications known to influence glucose tolerance
  • Have any complicating medical or psychological issues or abnormal clinical laboratory results that interfere with study conduct or cause increased risk. These include pre-existing cardiac disease, COPD, neurological, or clinically significant blood count abnormalities (such as lymphopenia, leukopenia, or thrombocytopenia).

Other

  • Females who are pregnant or lactating
  • Immunodeficiency or clinically significant chronic lymphopenia

Who the study is looking for

  • ≤ 7 months from type 1 diabetes diagnosis based on ADA criteria
  • \> 21 days from type 1 diabetes diagnosis or metabolically stable per study physician assessment
  • Males and females 6-55 years of age, inclusive, at time of screening visit
  • Peak MMTT stimulated C-peptide ≥ 0.2 pmol/ml
  • Females of child-bearing age must be willing to use effective birth control for 1 year (which may include abstinence) from screening visit and undergo regular pregnancy testing
  • Up to date for clinically recommended immunizations prior to screening
  • Willing to forgo live vaccines 3 months prior to the screening visit until three months following last study drug administration
  • Willing and able to give informed consent or have parent or legal guardian provide informed consent if the subject is \< 18 years of age
  • Weight ≥ 20 kg at baseline visit
  • HbA1c ≤ 8.5% at baseline visit
  • Positive for at least 1 diabetes autoantibody (excluding mIAA in those who have received ≥ 2 weeks of exogenous insulin therapy)

Age in the registry: 6 years to 55 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Medical College of Wisconsin
Coordinator of this site? Confirm its status
MilwaukeeUnited StatesUnknown status
Benaroya Research Institute
Coordinator of this site? Confirm its status
SeattleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.