drugset / Trial / NCT04629664

FX-322 in Adults With Severe Sensorineural Hearing Loss

NCT04629664 ↗

Phase 1 Completed 31 enrolled Frequency Therapeutics
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase 1b, prospective, randomized, double-blind, placebo-controlled, single-dose, multicenter, safety study of FX-322, administered by intratympanic injection, in adults with severe sensorineural hearing loss.

Timeline

Start
2020-11-02
Primary completion
2021-05-26
Completion
2021-09-20

Drugs

EvaluationDrugModalityDoseRoute
Comparator FX-322 Unknown — Other