Clinical Trials in the USA / NCT04480567
Active, not recruiting
Phase 1/2
AAV Gene Therapy Study for Subjects with PKU
NCT04480567 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Phenylketonuria (PKU)
Investigational drug(s) / intervention(s)
BMN 307
BMN 307: AAV Gene Therapy Infusion
Study summary
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.
Eligibility
Inclusion Criteria:
* Male and female subjects with diagnosis of PKU which is a condition characterized by PAH deficiency
* Ability and willingness to maintain dietary protein intake consistent with baseline intake
* Willingness to abstain from hepatotoxic substances post-BMN 307 administration
* Willingness and capable per investigator opinion to comply with study procedures and requirements
* Willingness to use effective methods of contraception
* Plasma Phe levels \> 600 µmol/L
Exclusion Criteria:
* Subjects with primary BH4 deficiency or other forms of BH4 metabolism deficiency
* Clinically significant liver dysfunction or disease
* Prior treatment with gene therapy
* Any condition that, in the opinion of the investigator or Sponsor, would prevent the subject from fully complying with the requirements of the study
* History of malignancy
Primary outcome measure(s)
- Change from baseline in mean Plasma Phe levels — baseline, week 12
Trial sites (3)
| Facility | City | Region | Status |
|---|---|---|---|
| University of South Florida | Tampa | Florida | |
| Morristown Medical Center | Morristown | New Jersey | |
| University Hospital Birmingham NHS Foundation Trust | Birmingham | United Kingdom |
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Other trials for the same condition
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04480567 on ClinicalTrials.gov ↗ ← All trials in the USA