drugset / Trial / NCT04133454

Evaluation of Safety and Tolerability of Libella Gene Therapy for Alzheimer's Disease: AAV- hTERT

NCT04133454 ↗

Phase 1 Unknown 5 enrolled Libella Gene Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

Using gene therapy to express active telomerase (hTERT) in human cells has the potential to treat many neurodegenerative diseases related to aging, including Alzheimer's disease (AD). This study will entail treating subjects with hTERT delivered via transduction using AAV. The goal is to extend the telomeres to prevent, delay, or even reverse the development of the pathology of AD. It is expected to have a direct consequence on cognitive function and quality of life in patients with neurodegenerative diseases, such as AD.

Timeline

Start
2019-10-10
Primary completion
2021-01
Completion
2021-01

Drugs

EvaluationDrugModalityDoseRoute
Subject AAV-hTERT Gene therapy (AAV / viral vector) — Intravenous

Indications