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Description of Patients With Type 1 Diabetes Treated With Teplizumab

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NCT06892002

Sponsored by Sanofi (industry) · SNY — their whole pipeline →.

Phase
Status
Completed
Study type
Observational
Enrollment
110actual
Sites
27
Countries
Israel, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-02-11actualWhen the study began enrolling
Primary completion2025-08-05actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-08-05actualThe whole study's end, after follow-up
First posted2025-03-24actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-08-15actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Type 1 Diabetes

Intervention

  • Drug: Teplizumab

Primary outcomes

what the primary-completion date above is the date OF
Participant demographic characteristics at teplizumab initiation
measured At Day 1 (first dose of teplizumab)
Participants' family history of T1D and autoimmune diseases
measured At Day 1 (first dose of teplizumab)
Presence of T1D susceptibility genes: Genetic risk score
measured At Day 1 (first dose of teplizumab)
Presence of T1D susceptibility genes: Human Leukocyte Antigen (HLA)-haplotype
measured At Day 1 (first dose of teplizumab)
Participants' medical history
measured From 6 months prior to the first dose of teplizumab (teplizumab initiation) (or the earliest date of all data contributing to Stage 2 T1D diagnosis, whichever is earlier) up to the medical records abstraction date, approximately 3-4 years
Assessment of blood glucose test results: CGM
measured At screening (6 months before teplizumab initiation), within 6 weeks prior to teplizumab initiation, during teplizumab infusion (2 weeks), following completion of teplizumab treatment (through study completion, up to 30 months)"

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