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

Sponsor

National Taiwan University Hospital (Other)

Overall Status

Active, not recruiting

CT.gov ID

NCT01395641

Collaborator

(none)

Enrollment

Location

Arm

Anticipated Duration (Months)

0.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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

Condition or Disease	Intervention/Treatment	Phase
Aromatic L-amino Acid Decarboxylase (AADC) Deficiency	Drug: gene therapy	Phase 1/Phase 2

Detailed 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. 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.

Study Design

Study Type:

Interventional

Actual Enrollment :

10 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

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

Actual Study Start Date :

Oct 1, 2014

Anticipated Primary Completion Date :

Dec 31, 2021

Anticipated Study Completion Date :

Dec 31, 2021

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Gene therapy Intracerebral infusion of AAV2-hAADC viral vector will be performed	Drug: gene therapy AAV2-hAADC viral vector will be injected into bilateral putamen by stereotactic surgery. Other Names: Intracerebral infusion of AAV2-hAADC viral vector

Arm

Intervention/Treatment

Experimental: Gene therapy

Intracerebral infusion of AAV2-hAADC viral vector will be performed

Drug: gene therapy

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

Other Names:

Intracerebral infusion of AAV2-hAADC viral vector

Outcome Measures

Primary Outcome Measures

Evaluation of therapeutic effect [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 Outcome Measures

Evaluation of safety and other therapeutic effects Evaluation for the treatment safety [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).
Evaluation of secondary therapeutic effects [5 years]
Weight gain Increased signal intensity of dopamine in putamen during PET imaging Increased score in other development evaluations
Exploratory endpoint [5 years]
The correlation between anti-AAV2 titer and therapeutic effect The correlation between subject's age and therapeutic effect

Eligibility Criteria

Criteria

Ages Eligible for Study:

24 Months and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

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.