This is a Phase 1/2, open-label, dose escalation study to evaluate the safety, efficacy and tolerability of BMN 307 in adult PKU subjects with PAH deficiency. Participants will receive a single administration of BMN 307 and will be followed for safety and efficacy.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
100
AAV Gene Therapy Infusion
University of South Florida
Tampa, Florida, United States
Morristown Medical Center
Morristown, New Jersey, United States
University Hospital Birmingham NHS Foundation Trust
Birmingham, United Kingdom
Change from baseline in mean Plasma Phe levels
Time frame: baseline, week 12
Change from baseline in mean Plasma Phe levels
Time frame: baseline, week 96
Change from baseline in dietary protein intake from intact food
Time frame: baseline, week 96
Number of participants with treatment-emergent adverse event
Time frame: At 5 years
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