Skip to main content
OpenTrials
Completed

NCT Number: NCT01267422

Safety and Efficacy Study of rAAV2-ND4 Treatment of Leber Hereditary Optic Neuropathy (LHON)

This study is meant to assess the safety and efficacy of rAAV2-ND4 treatment of Leber hereditary optic neuropathy with 11778 LHON mutation.

Completed

Looking for future studies?

Notify Me

Key information

About this study

Leber's Hereditary Optic Neuropathy (LHON) is a maternally inherited ocular disorder associated with a mutation in mtDNA . The common manifestation is visual loss which caused by the respiratory chain enzymes complex dysfunction resulting in increased oxidative stress enzymes production.

Material and Method Seven patients with 11778 LHON mutation were randomly treated with a Single IVT Injection of recombinant Adeno-Associated Virus-NADH dehydrogenase, subunit 4 (complex I)(rAAV2-ND4)(0.05ml).The dose was 5 × 10^9 vg/0.05 mL for patients younger than 12 years old, and 1 × 10^10 vg/0.05 mL for patients older than 12 years old. The visual acuity, visual evoked potential (VEP),optical coherence tomography( OCT), computerized visual field, electroretinograms(ERG), retinal nerve fiber layer(RNFL)and Liver and kidney function in plasma were compared before and after treatment at 1,3,and 6, months interval.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • comply with Leber hereditary optic neuropathy diagnostic criteria.
  • in patients with informed consent, voluntary participation.
  • signed informed consent.
  • 8 ≤ Age ≤ 60 years old, good health, the patient can tolerate local anesthesia surgery.
  • to comply with doctor's instructions, can in the time of referral.

Exclusion criteria

  • Cardiopulmonary and renal function in severe weakness, cancer, a variety of bleeding disorders, acute sensing disease, high fever, high fever disease, women during pregnancy, heart disease, such as post-operative recovery period.
  • Are participating in other clinical studies of patients.
  • Patients with mental disorders.

Treatment and study plan

rAAV2-ND4

Drug

injection

Other names: rAAV2-ND4 gene therapy

Primary outcomes

  1. The Best Corrected Visual Acuity(BCVA)

    Time frame: Up to 3 years

  2. Results of CD3/CD4/CD8 Test

    Time frame: up to 6 months

    The mean percentage of CD3+/CD4+/CD8+ test before and after treatment

Secondary outcomes

  1. Intraocular Pressure;

    Time frame: Up to 3 years

  2. Neutralizing Antibody Assay

    Time frame: up to 3 years

    The mean of Neutralizing antibody assay of 8 patients before and after treatment

  3. Average RNFL Thickness Througth Optical Coherence Tomography(OCT) Test

    Time frame: Up to 3 years

    Average RNFL thickness of 8 patients througth Optical coherence tomography(OCT) test before and after treatment

  4. Computerized Visual Field(MD: Mean Deviation, the Value Close to 0 Regarded Normal)

    Time frame: up to 3 years

    MD: mean deviation, the value Close to 0 regarded normal.VFI/MD:The bigger one was more close to the normal value.

  5. Computerized Visual Field(VFI: Visual Field Index ,the Value Close to 100% Regarded Normal)

    Time frame: up to 3 years

    VFI: visual field index ,the value Close to 100% regarded normal. VFI/MD:The bigger one was more close to the normal value.

Sponsors and collaborators

Lead sponsor

Bin Li

Other

Collaborators

  • Huazhong University of Science and Technology

Registry information

Official study title

Safety and Efficacy Study of a Single Intravitreal Injection of rAAV2-ND4 Treatment of Leber Hereditary Optic Neuropathy

Acronym: rAAV2-ND4

Important dates

Study start
2011
Primary completion
2015
Study completion
2015
First posted
Dec 28, 2010
Registry last updated
Jan 31, 2018

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.

Published trials that share one or more normalized conditions with this study.