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Registry for Stage 2 Type 1 Diabetes

RecruitingObservational study

An Observational, Long-term Safety Study of TZIELD® (Teplizumab-mzwv) in Patients With Stage 2 Type 1 Diabetes

Who can join

All ages · All sexes

Full eligibility criteria
Inclusion Criteria:

TZIELD-Exposed Cohort

* Patients in the US diagnosed with Stage 2 T1D who are planned to initiate TZIELD treatment according to the currently approved label or who have initiated TZIELD treatment within 6 months prior to enrollment:
* Day 1: 65 mcg/m2
* Day 2: 125 mcg/m2
* Day 3: 250 mcg/m2
* Day 4: 500 mcg/m2
* Days 5 through 14: 1,030 mcg/m2 per day
* Cumulative dose is approximately 11,240 mcg/m2
* Appropriate written informed consent/assent as applicable for the age of the patient

TZIELD-Unexposed Cohort

* Patients in the US diagnosed with Stage 2 T1D but who are not treated with TZIELD
* Appropriate written informed consent/assent as applicable for the age of the patient

Exclusion Criteria:

* Patients who initiated TZIELD treatment more than 6 months prior to enrollment
* Patients who had participated in a previous clinical trial for TZIELD
* Patients in an ongoing clinical trial of an investigational product or who had ended participation within 6 months prior to study enrollment; patients participating in other observational studies may be enrolled

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

About the study

Stage 2 Type 1 Diabates (T1D) is an early stage of T1D characterized by dysglycemia but not yet leading to clinical symptoms. Progression of the disease to Stage 3 (clinical T1D), leads to overt hyperglycemia requiring eventually exogenous insulin.

TZIELD® (teplizumab-mzwv) has been approved to delay onset of stage 3 T1D, by the United States (US) Food and Drug Administration (FDA) for adults and children aged 8 years and older with Stage 2 T1D.

The purpose of this study is to collect general information on patients with stage 2 T1D and further information on the long-term effects of TZIELD® in patients with Stage 2 T1D, treated as per standard of care.

What is being tested

Sponsor: Sanofi · Participants: 200 · Started: Sep 27, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06481904

Locations in the U.S.

CaliforniaUniversity of California Los Angeles Health- Site Number : 8400020, Los Angeles
University of California San Francisco - Mission Bay- Site Number : 8400005, San Francisco
ColoradoUniversity of Colorado Hospital- Site Number : 8400026, Aurora
ConnecticutYale University School of Medicine- Site Number : 8400025, New Haven
FloridaUniversity of Florida Health- Site Number : 8400035, Gainesville
Nemours Children's Speciality Care- Jacksonville- Site Number : 8400006, Jacksonville
Nicklaus Children's Hospital - Miami - Southwest 62nd Avenue- Site Number : 8400034, Miami
University of Miami Miller School of Medicine- Site Number : 8400037, Miami
University of South Florida- Site Number : 8400022, Tampa
GeorgiaMidtown Medical Center - Columbus- Site Number : 8400013, Columbus
IllinoisUniversity of Chicago Medical Center- Site Number : 8400017, Chicago
IndianaIndiana University Health Riley Hospital for Children- Site Number : 8400004, Indianapolis
KentuckyNorton Brownsboro Hospital- Site Number : 8400030, Louisville
MarylandJohns Hopkins School of Medicine- Site Number : 8400031, Baltimore
MichiganUniversity of Michigan Health System - Ann Arbor- Site Number : 8400028, Ann Arbor
Associated Endocrinologists, PC- Site Number : 8400039, Farmington Hills
Corewell Health - Grand Rapids - Michigan Street Northeast- Site Number : 8400009, Grand Rapids
MinnesotaMayo Clinic- Site Number : 8400010, Rochester
MissouriChildren's Mercy Adelle Hall Campus- Site Number : 8400014, Kansas City
New YorkWomen & Children's Hospital of Buffalo- Site Number : 8400018, Buffalo
Feinstein Institute for Medical Research (Northwell)- Site Number : 8400016, Manhasset
Ten's Medical PC- Site Number : 8400027, Staten Island
SUNY Upstate Medical University - Syracuse- Site Number : 8400007, Syracuse
North CarolinaUNC Children's Hospital- Site Number : 8400008, Chapel Hill
OhioCincinnati Children's Hospital Medical Center- Site Number : 8400024, Cincinnati
Rainbow Babies And Children's Hospital- Site Number : 8400011, Cleveland
The Ohio State University- Site Number : 8400032, Columbus
PennsylvaniaHospital of The University of Pennsylvania- Site Number : 8400021, Philadelphia
The Children's Hospital of Philadelphia- Site Number : 8400029, Philadelphia
TennesseeAM Diabetes & Endocrinology Center- Site Number : 8400012, Bartlett
Vanderbilt University Medical Center- Site Number : 8400023, Nashville
TexasTexas Diabetes & Endocrinology - Austin - North Mopac Expressway- Site Number : 8400040, Austin
University of Texas - Southwestern Medical Center- Site Number : 8400003, Dallas
Cook Children's- Site Number : 8400038, Fort Worth
Texas Children's Hospital- Site Number : 8400002, Houston
UtahUniversity of Utah Health Hospital- Site Number : 8400019, Salt Lake City
West VirginiaUnited BioSource Corporation- Site Number : 8400001, Morgantown

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.