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NCT Number: NCT01395641

A Phase I/II Clinical Trial for Treatment of Aromatic L-amino Acid Decarboxylase (AADC) Deficiency Using AAV2-hAADC

This Phase I/II trial is to prove the efficacy and safety of AAV2-hAADC to treat patients with AADC deficiency.

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Key information

Conditions

Aromatic L-amino Acid Decarboxylase (AADC) Deficiency Aromatic amino acid decarboxylase deficiency

Age range

24 month and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

National Taiwan University Hospital

Taipei, 100, Taiwan

About this study

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. Taiwanese carry a high prevalence of AADC deficiency due to the founder mutation IVS6+4 A>T, and patients usually die before the age 5-6 years due to severe motor dysfunction.

Gene therapy with adeno-associated virus (AAV) serotype 2 (AAV2) driven human AADC (hAADC) has been tested in both animal models and Phase I clinical trials of Parkinson disease. We have done a compassionate treatment of 8 patients with AADC deficiency by AAV2-hAADC and demonstrated a result that among the treated patients, 4 could stand with support, 3 could sit with support, and there was no virus-associated toxicity. The longest follow up has exceeded 4 years.

This study is to prove the safety and efficacy of AAV2-hAADC treatment for patients with Aromatic L-amino acid decarboxylase (AADC) deficiency.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • With a confirmed diagnosis of AADC, including cerebrospinal fluid analysis to show reduced levels of neurotransmitter metabolites, HVA and 5-HIAA, and higher L-Dopa, together with more than one mutation within AADC gene.
  • Classical clinical characteristics of AADC deficiency, such as oculogyric crises, hypotonia and developmental retardation.
  • The sick child has to be over 2 years old or a head circumference big enough for surgery.
  • Participating patients must cooperate completely for all evaluations and examinations before, during and after the whole trial.
  • Parents or guardians must sign to agree on this informed consent.

Exclusion criteria

  • Significant brain structure abnormality
  • Patients with any health or neurological doubts that may increase the risk of surgery cannot join this trial. PI has the right to evaluate the feasibility of subjects for this trial based on his/her health condition.
  • Since high-level neutralizing antibodies may disturb the therapeutic effect of gene therapy, patients with anti-AAV2 neutralizing antibody titer over 1,200 folds or an ELISA OD over 1 cannot be enrolled into this trial.
  • Subjects enrolled in this clinical trial cannot take any medications that may affect this trial.

Treatment and study plan

gene therapy

Drug

AAV2-hAADC viral vector will be injected into bilateral putamen by stereotactic surgery.

Other names: Intracerebral infusion of AAV2-hAADC viral vector

Primary outcomes

  1. Evaluation of therapeutic effect

    Time frame: 12 months

    • At one year post-surgery, neurotransmitter metabolites (HVA or HIAA) is detectable in CSF (higher than that at pre-surgery)
    • At one year post-surgery, PDMS-II score is higher than that at pre-surgery, with an improvement over 10 points

Secondary outcomes

  1. Evaluation of safety and other therapeutic effects Evaluation for the treatment safety

    Time frame: 12 months

    • The absence of intracranial bleeding, which requires surgical management, after the surgery
    • Craniotomy-induced CSF exudation
    • The severity of post-surgery hyperactivity (if feeding is affected and then nasogastric tube is needed)
    • Incidence of other severe adverse events (information of adverse events of all kinds and severities will be collected, including treatment-emergent adverse events).

  2. Evaluation of secondary therapeutic effects

    Time frame: 5 years

    • Weight gain
    • Increased signal intensity of dopamine in putamen during PET imaging
    • Increased score in other development evaluations

  3. Exploratory endpoint

    Time frame: 5 years

    • The correlation between anti-AAV2 titer and therapeutic effect
    • The correlation between subject's age and therapeutic effect

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Collaborators

  • PTC Therapeutics

Registry information

Acronym: AADC

Important dates

Study start
2014
Primary completion
2020
Study completion
2022
First posted
Jul 15, 2011
Registry last updated
Feb 10, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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