Status: Recruiting
Safety and Efficacy Study of NGGT002 in cPKU Adult Subjects
This is a Phase 1/2, open-label, multiple-center, dose escalation and cohort expansion study to evaluate the safety and efficacy of NGGT002 in adult subjects with classic Phenylketonuria (PKU). NGGT002 is a rAAV8 based vector carrying a functional copy of the human PAH gene. Participants will receive a single administration of NGGT002 and will be followed for safety and efficacy for 5 years.
Participants needed: 18
Trial details
Phase: Phase 1, Phase 2Age: 18-55Biological sex: AllType: InterventionalSponsor: NGGT (Suzhou) Biotechnology Co., Ltd.Updated: Nov 14, 2024Locations: 2
Eligibility criteria
Voluntarily participating in the study and signing the informed consent form; [+6]
Presence of anti-AAV8 neutralizing antibodies(≥1:5) [+23]