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Clinical Trial Summary

This trial includes dose-escalating part (phase 1) and dose confirming part, to prove the safety and efficacy of VGN-R09b to treat patients with severe AADC deficiency


Clinical Trial Description

Aromatic L-amino acid decarboxylase (AADC) is an enzyme responsible for the final step in the synthesis of neurotransmitters dopamine and serotonin. AADC deficiency is a rare genetic disorder. VGN-R09b is a kind of Gene therapy with adeno-associated virus (AAV) serotype 9 (AAV9) driven human AADC (hAADC) being injected directly into putamen. This is an open, dose-escalating and dose confirming study. The sponsor plans to explore two dose levels (6.0×1011vg and 1.28×1012vg) in dose-escalating phase (three subjects each cohort), then plans to have 10 subjects enrolled for dose confirmation phase. This study is to give evidence for the safety and efficacy of VGN-R09b treatment for patients with severe Aromatic L-amino acid decarboxylase (AADC) deficiency. ;


Study Design


Related Conditions & MeSH terms

  • Aromatic L-amino Acid Decarboxylase Deficiency

NCT number NCT06432140
Study type Interventional
Source Shanghai Vitalgen BioPharma Co., Ltd.
Contact Xiumin Wang, MD
Phone +86-18017395221
Email GCPwxm666@163.com
Status Not yet recruiting
Phase Phase 1
Start date May 2024
Completion date September 2030

See also
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Recruiting NCT05211609 - Prevalence of High Plasmatic 3OMethyldopa Level in a Specific Population of Patients With a Symptomatology Compatible With AADC Deficiency N/A
Completed NCT02399761 - Newborn Screening for Aromatic L-amino Acid Decarboxylase Deficiency N/A