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Recent-Onset Type 1 Diabetes Trial Evaluating Efficacy and Safety of Teplizumab

Sponsored by Provention Bio, Inc.

About this trial

Last updated a year ago

Study ID

PRV-031-001

Status

Completed

Type

Interventional

Phase

Phase 3

Placebo

Yes

Accepting

18-75 Years
8 to 17 Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 2 years ago

What is this trial about?

The purpose of this study is to determine whether teplizumab slows the loss of β cells and preserves β cell function in children and adolescent 8-17 years old who have been diagnosed with T1D in the previous 6 weeks.. Subjects will receive two courses of either teplizumab or placebo treatment 6 months apart.

What are the participation requirements?

Yes

Inclusion Criteria

1. Is 8 to 17 years of age, inclusive, at the time of randomization/initiation of study drug administration.

2. Has received a diagnosis of type 1 diabetes (T1D) according to the criteria from the American Diabetes Association.

3. Is able to be randomized and initiate study drug within 6 weeks (42 days) of the formal T1D diagnosis.

4. Has a peak stimulated C-peptide of ≥0.2 pmol/mL from a mixed meal tolerance test (MMTT) at screening.

5. Has a positive result on testing for T1D-related autoantibodies.

No

Exclusion Criteria

1. Has any autoimmune disease other than T1D with the exception of stable thyroid or celiac disease.

2. Has an active infection and/or fever.

3. Has a history of or serologic evidence at screening of current or past infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV).

4. An individual who has a medical, psychological or social condition that, in the opinion of the Principal Investigator, would interfere with safe and proper completion of the trial.

Locations

Location

Status