The 812P401 Study is a clinical research study evaluating an investigational medication (SPN‑812) to see if it may help reduce ADHD symptoms in preschool-age children. SPN-812 is approved by the U.S. Food and Drug Administration (FDA) as Qelbree and is used for the treatment of ADHD in pediatric patients ages 6 to 17.
The study lasts about 10 weeks and includes clinic visits, ADHD evaluations, and study-related care at no cost. Families who qualify may also be eligible to join an optional extension study where all children receive the active medication.
Conducted in Atlanta, GA 30318, United States
Children between 4 years 0 months and 5 years 9 months may qualify.
Study lasts about 10 weeks with ~8 clinic visits
Families may receive up to $825 for participation
Families may receive up to $825 for completing all study visits.
All ADHD evaluations, physical exams, study medication, and study-related care are provided at no cost.
Travel reimbursement may also be available.
This is an opportunity to contribute to research on ADHD in preschoolers while receiving close medical oversight and support from experienced professionals.
About 10 weeks, including screening, 6 weeks of treatment, and a follow-up call.
There is no cost. All study-related evaluations, care, and medication are provided free of charge.
During the main study, children are randomly assigned to SPN‑812 or placebo. After completing the study, you may enroll your child in an extension study with active medication only.
Families may receive up to $825 for participation and may be reimbursed for certain study-related expenses.