FX-322 in Adults With Severe Sensorineural Hearing Loss

Status Completed

Clinical Trial 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.

Clinical Trial Description

This is a Phase 1b placebo-controlled, double-blind, single-dose safety study of intratympanic FX-322 dosed in subjects with severe sensorineural hearing loss. Approximately 30 subjects are planned to be enrolled in this study. The subjects will be randomized to receive one dose FX-322 (24) or placebo (6) and will return for safety, otologic, and audiologic assessments at Days 30 and 90 after the study injection. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04629664
Study type	Interventional
Source	Frequency Therapeutics
Contact
Status	Completed
Phase	Phase 1
Start date	November 2, 2020
Completion date	September 20, 2021

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