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Long-Term Outcomes of Teplizumab in Routine Clinical Care

RecruitingObservational study

Long-Term Outcomes of Participants Treated With Teplizumab in Routine Clinical Care

Who can join

All ages · All sexes

Full eligibility criteria
Inclusion Criteria -

* Participants who have received at least 1 teplizumab infusion within 6 weeks prior to enrollment.
* Participants must have a confirmed diagnosis of Stage 2 T1D according to the treating physician at the time of the first infusion of teplizumab.

(Note: Participants who progress to Stage 3 T1D by Week 6 will still be eligible, provided they were in Stage 2 at the time of the first teplizumab infusion.)

• Participants (or their legal guardians, as applicable) who provide appropriate written or electronic informed consent/assent as applicable for the age of the participant and as per local regulations.

Exclusion Criteria -

* Participants who had participated in a previous clinical trial for teplizumab.
* Participants enrolled in a clinical trial within 6 months prior to study enrollment.

(Note: Participants enrolled in other observational studies may be included.)

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

About the study

This is an observational, prospective cohort study designed to evaluate the outcomes after teplizumab treatment in participants with Stage 2 Type 1 Diabetes (T1D) for delaying the onset of Stage 3 T1D. The study will monitor participants receiving teplizumab as part of routine clinical care across multiple sites. Additionally, patient-reported outcomes (PROs) will be evaluated to further assess the treatment's impact on participant's quality of life including emotional and psychosocial aspects associated with T1D. This approach will provide a more comprehensive understanding of how the treatment performs over time and across diverse patient populations, providing valuable insights into the sustained effects of teplizumab and offering a real world picture of its impact on the long-term management of T1D.

What is being tested

Sponsor: Sanofi · Participants: 1,000 · Started: Mar 19, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07360080

Locations in the U.S.

GeorgiaInvestigational Site Number: 8400003, Atlanta
Investigational Site Number: 8400004, Atlanta
New YorkInvestigational Site Number: 8400001, New York
Investigational Site Number: 8400002, Syosset
UtahInvestigational Site Number: 8400005, Sandy City

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.