A Phase III Study to Investigate the Impact of Diamyd in Patients Newly Diagnosed With Type 1 Diabetes (USA)- DIAPREVENT
Type 1 Diabetes Mellitus
About this trial
This is an interventional treatment trial for Type 1 Diabetes Mellitus focused on measuring Diabetes, Juvenile Diabetes, Diabetes type 1, Autoimmune Diabetes, Insulin dependent Diabetes, Type 1 diabetes, Type 1 diabetes mellitus, Diamyd, rhGAD65, GAD, GAD-alum
Eligibility Criteria
Main Inclusion Criteria:
- Insulin dependent type 1 diabetes mellitus diagnosed within the previous 3 months at time of screening
- Fasting C-peptide level at time of screening above 0.1 nmol/L
- Elevated GAD65 antibodies (GADA) at time of screening
- Male and female patients between 10 and 20 years of age
Main Exclusion Criteria:
- Treatment with immunosuppressants or any anti-diabetic medications other than insulin
- A history of certain diseases or conditions (e.g. anemia, HIV, hepatitis, epilepsy, head trauma, neurological diseases or cerebrovascular accident, alcohol or drug abuse etc)
- Treatment with any vaccine within 1 month prior to planned first Diamyd dose or planned treatment with vaccine up to 2 months after the last injection with Diamyd, excluding the influenza vaccine
- Participation in other clinical trials with a new chemical entity within the previous 3 months
- Pregnancy or planned pregnancy within 1 year after the last Diamyd dose
- Presence of associated serious disease or condition which in the opinion of the investigator makes the patient non-eligible for the study
Sites / Locations
- University of Arizona
- Arkansas Children's Hospital Research Institute
- Alex Endocrine Associates
- Children's Hospital Orange County
- Rady Children's Hospital
- Stanford University Medical Center
- Barbara Davis Center for Childhood Diabetes
- Christina Care Research institute
- University of Florida
- Nemours Children's Clinic
- Miami Children's Hospital Research Institute
- University of South Florida
- Atlanta Diabetes Associates
- Rocky Mountain Diabetes and Osteoporosis Center
- University of Iowa Hospitals and Clinicals
- Mid America Diabetes Associates
- University of Kentucky College of Medicine
- University of Louisville Research Foundation
- Children's Hospital
- University of Maryland Medical Center
- Tufts Medical Center
- UMass Memorial Medical Center
- University of Michigan Health System
- Alzohaili Medical Consultants
- The Children's Mercy Hospital
- St. Louis Children's Hospital
- Creighton Diabetes Center
- Kathryn Eckert
- Hackensack University Medical Center
- Morristown Memorial Hospital
- Winthrop University Hospital
- Naomi Berrie Diabetes Center of Columbia University
- University of Rochester
- SUNY Institute for Human Performance
- Children's Hospital Medical Center of Akron
- University of Oklahoma, Schustermann Center Clinic
- Children's Hospital of Pittsburgh of UPMC
- Regional Medical Clinic - Endocrinology
- LeBonheur Children's Medical Center
- Cook Children's Medical Center
- CHRISTUS Santa Rosa Children's Hospital
- Virginia Commonwealth University
- Benaroya Research Institute
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Placebo Comparator
A
B
C
This arm will receive 2 subcutaneous injections with 20 µg Diamyd on days 1 and 30, i.e., 1 prime and 1 booster dose, followed by 2 additional single doses with Diamyd 20 µg on days 90 and 270.
This arm will receive 2 subcutaneous injections with 20 µg Diamyd on days 1 and 30, i.e., 1 prime and 1 booster dose, followed by 2 additional single doses with placebo on days 90 and 270.
This arm will receive 4 injections of placebo, 1 each on days 1, 30, 90 and 270.