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Direct CNS Administration of a Replication Deficient Adeno-associated Virus Gene Transfer Vector Serotype rh.10 Expressing the Human CLN2 cDNA to Children With LINCL With Uncommon Genotypes and/or Moderate to Severe Impairment

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Direct CNS Administration of a Replication Deficient Adeno-associated Virus Gene Transfer Vector Serotype rh.10 Expressing the Human CLN2 cDNA to Children With LINCL With Uncommon Genotypes and/or Moderate to Severe Impairment

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 07 Nov 2021

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At a glance

  • Drugs CLN2 gene therapy (Primary)
  • Indications Neuronal ceroid lipofuscinosis
  • Focus Therapeutic Use

    • Most Recent Events

    • 13 Feb 2020 Status changed from active, no longer recruiting to completed.
    • 08 Jan 2018 Status changed from recruiting to active, no longer recruiting.
    • 16 Aug 2012 Planned End Date changed from 1 Dec 2011 to 1 Dec 2022 as reported by ClinicalTrials.gov.

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