drugset / Trial / NCT04133649

Evaluation of Safety and Tolerability of Libella Gene Therapy for the Treatment of Aging: AAV- hTERT

NCT04133649 ↗

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

Summary

Using gene therapy to express active telomerase (hTERT) in humans has the potential to treat many of the age related diseases, including Aging itself. 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 Aging.

Timeline

Start
2019-10-17
Primary completion
2021-01
Completion
2021-01

Drugs

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

Indications

No indication recorded.