What is the purpose of the Angelman syndrome study?
The purpose of the study is to look at the safety, tolerability, and efficacy of NNZ-2591 in the treatment of children with Angelman syndrome.
This study investigates an oral medication called “NNZ-2591”, which aims to improve the impaired connections and signalling between brain cells that are involved in Angelman syndrome. The study medication is experimental.
What does the study involve?
Participation in the study will be required for approximately 19 weeks, with a combination of in-clinic, remote, and telehealth consultations. An in-home nurse will also visit your house to check on the participant and administer a number of assessments.
Participants in the Angelman study will need to:
Is there a cost?
There is no cost to participate in this clinical trial.
Reimbursement is available for reasonable* travel and incidental costs incurred attending your clinic visits.
* In accordance with ATO schedules on reasonable allowances (Tax Determination 2021/16)
Who is eligible for this study?
Potential participants must:
Specific details on the eligibility criteria can be found at www.clinicaltrials.gov
The clinical team managing the study at one of the participating sites will determine if your child is eligible to enrol. For more information, please speak with one of the participating site teams.