This study will be the first evaluation of Symlin in adolescent subjects with type 1 diabetes mellitus and is designed to evaluate the blood levels (pharmacokinetics), biochemical and physiological effects (pharmacodynamics), and safety and tolerability of Symlin in these subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
12
single subcutaneous doses of 15mcg and 30mcg
Research Site
Aurora, Colorado, United States
Research Site
Kansas City, Missouri, United States
Research Site
New York, New York, United States
To evaluate the pharmacokinetics of Symlin in adolescent subjects with type 1 diabetes
Time frame: single doses
To assess the safety and tolerability of Symlin in adolescent subjects with type 1 diabetes
Time frame: single doses
To evaluate the effects of Symlin compared to placebo in adolescent subjects with type 1 diabetes on various pharmacodynamic endpoints
Time frame: single doses
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.