Clinical Study: Type 1 Diabetes (T1D)
SAFEGAURD
SAFety and Efficacy of Human Anti-thymocyte ImmunoGlobUlin SAB-142 ARresting Progression of Type 1 Diabetes
Status: Enrolling
Email: diabetes@benaroyaresearch.org
Phone: (800) 888-4187
Study Summary
The SAFEGUARD study will evaluate the safety and efficacy of an investigational medicine called SAB-142 in delaying disease progression in people newly diagnosed with T1D.
Ages 15-40 will be enrolled first, followed by 5 to 40-year-olds later in the study.
Eligibility Criteria
You/your child may qualify to participate in the SAFEGUARD clinical study if the following criteria are met:
- Aged between 5 to 40 years, inclusively
- Newly diagnosed with T1D (enrolled in the study within 100 days of diagnosis)
What will study participants be asked to do?
If you/your child qualify to participate:
- You/they will be assigned to either Part A or Part B treatment, depending on when you/they are enrolled into the study.
- For both Part A and Part B, all groups will receive 2 treatment courses, 6 months apart. Each treatment course will be given via intravenous infusion (i.e. via a small tube placed into a vein) over 2 days.
- There will be 7 scheduled follow-up visits and 3 phone calls to monitor the safety and efficacy of the treatment
- You/your child will NOT be charged for the study medicine or placebo, study visits, or tests and procedures needed for the study
- You/your child are free to leave the study at any time
For more information visit: https://clinicaltrials.gov/study/NCT07187531