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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
- TZIELD (teplizumab-mzwv) (drug)
Sponsor: Sanofi · Participants: 200 · Started: Sep 27, 2024
Contact the study team
- Trial Transparency email recommended (Toll free for US & Canada) · Phone: 800-633-1610
Official record on ClinicalTrials.gov — NCT06481904
Locations in the U.S.
| California | University of California Los Angeles Health- Site Number : 8400020, Los Angeles University of California San Francisco - Mission Bay- Site Number : 8400005, San Francisco |
| Colorado | University of Colorado Hospital- Site Number : 8400026, Aurora |
| Connecticut | Yale University School of Medicine- Site Number : 8400025, New Haven |
| Florida | University 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 |
| Georgia | Midtown Medical Center - Columbus- Site Number : 8400013, Columbus |
| Illinois | University of Chicago Medical Center- Site Number : 8400017, Chicago |
| Indiana | Indiana University Health Riley Hospital for Children- Site Number : 8400004, Indianapolis |
| Kentucky | Norton Brownsboro Hospital- Site Number : 8400030, Louisville |
| Maryland | Johns Hopkins School of Medicine- Site Number : 8400031, Baltimore |
| Michigan | University 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 |
| Minnesota | Mayo Clinic- Site Number : 8400010, Rochester |
| Missouri | Children's Mercy Adelle Hall Campus- Site Number : 8400014, Kansas City |
| New York | Women & 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 Carolina | UNC Children's Hospital- Site Number : 8400008, Chapel Hill |
| Ohio | Cincinnati 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 |
| Pennsylvania | Hospital of The University of Pennsylvania- Site Number : 8400021, Philadelphia The Children's Hospital of Philadelphia- Site Number : 8400029, Philadelphia |
| Tennessee | AM Diabetes & Endocrinology Center- Site Number : 8400012, Bartlett Vanderbilt University Medical Center- Site Number : 8400023, Nashville |
| Texas | Texas 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 |
| Utah | University of Utah Health Hospital- Site Number : 8400019, Salt Lake City |
| West Virginia | United 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.