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Gene Therapy for Tay-Sachs Disease

Plain-language summary

This study investigates a gene therapy for Tay-Sachs disease. Anyone diagnosed with a hexosaminidase deficiency disease could be included. The study was carried out as a non-phase study and has been completed.

The summary above is a plain-language rendering of the official record. The original English title is shown for reference.

Trial details

Phase
N/A
Status
Completed
Sponsor
University of Minnesota
Start date
12/1/2010
Estimated completion
8/1/2014
Countries
United States

Related genes

Locations

  • Tampa, United States
  • Minneapolis, United States

Eligibility criteria

Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.

Inclusion Criteria:

Any person who has been diagnosed with a hexosaminidase deficiency disease can be included in this study.

Exclusion Criteria:

The only exclusion criteria is a desire not to participate in this study.
This is not medical advice. Consult your specialist.
View the official record on ClinicalTrials.gov →