drugset / Trial / NCT04601909

FX-322 in Adults With Age-Related Sensorineural Hearing Loss

NCT04601909 ↗

Phase 1 Completed 30 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 age-related sensorineural hearing loss.

Timeline

Start
2020-09-17
Primary completion
2022-05-16
Completion
2022-05-16

Drugs

EvaluationDrugModalityDoseRoute
Comparator FX-322 Unknown — Other