The goal of this clinical trial is to learn if MZ-1866 is a safe and tolerable treatment for children and adults with Pitt Hopkins Syndrome. To evaluate the safety of MZ-1866, the following will be evaluated: * frequency and severity of adverse events * physical exam, laboratory results and electrocardiogram findings Participants will: * receive a single dose of MZ-1866 by intracerebroventricular injection * be seen by the study physician and site staff periodically to assess changes to their health status * be periodically evaluated using neurodevelopmental tools Caregivers will: * be interviewed periodically about the health status and development of the participant * keep diaries and complete periodic questionnaires regarding participant symptoms
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
12
AAV-9 gene therapy delivered by intracerebroventricular injection
UCSF Benioff Children's Hospital Oakland
Oakland, California, United States
Rush University Medical Center
Chicago, Illinois, United States
To evaluate the safety and tolerability of MZ-1866 in participants with Pitt Hopkins Syndrome
Frequency and severity of adverse events of special interest
Time frame: Week 104
To evaluate the safety and tolerability of MZ-1866 in participants with Pitt Hopkins Syndrome
Frequency and severity of adverse events
Time frame: Week 104
To further assess the safety and tolerability of MZ-1866 in participants with Pitt Hopkins Syndrome
Frequency of clinically significant physical examination findings, vital signs, laboratory tests and electrocardiograms that are considered outside normal range.
Time frame: Week 104
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