ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

FX-322 in Adults With Acquired Sensorineural Hearing Loss

ClinicalTrials.gov ID: NCT05086276

Public ClinicalTrials.gov record NCT05086276. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 20, 2026, 11:35 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Prospective, Randomized, Double-Blind, Placebo-Controlled, Single-Dose, Multicenter Study to Evaluate the Efficacy of FX-322 Administered by Intratympanic Injection in Adults With Acquired Sensorineural Hearing Loss

Study identification

NCT ID
NCT05086276
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Frequency Therapeutics
Industry
Enrollment
142 participants

Conditions and interventions

Interventions

  • FX-322 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 11, 2021
Primary completion
Dec 29, 2022
Completion
Dec 29, 2022
Last update posted
Apr 20, 2023

2021 – 2022

United States locations

U.S. sites
26
U.S. states
16
U.S. cities
26
Facility City State ZIP Site status
Clinical Trial Site Tucson Arizona 00000
Clinical Trial Site Fresno California 00000
Clinical Trial Site Torrance California 00000
Clinical Trial Site Colorado Springs Colorado 00000
Clinical Trial Site Sarasota Florida 00000
Clinical Trial Site Tampa Florida 00000
Clinical Trial Site Marrero Louisiana 00000
Clinical Trial Site Novi Michigan 00000
Clinical Trial Site Omaha Nebraska 00000
Clinical Trial Site Albany New York 00000
Clinical Trial Site Amherst New York 00000
Clinical Trial Site New York New York 00000
Clinical Trial Site Winston-Salem North Carolina 00000
Clinical Trial Site Cincinnati Ohio 00000
Clinical Trial Site Oklahoma City Oklahoma 00000
Clinical Trial Site Charleston South Carolina 00000
Clinical Trial Site Orangeburg South Carolina 00000
Clinical Trial Site Spartanburg South Carolina 00000
Clinical Trial Site Dallas Texas 00000
Clinical Trial Site Fort Worth Texas 00000
Clinical Trial Site San Antonio Texas 00000
Clinical Trial Site Murray Utah 00000
Clinical Trial Site St. George Utah 00000
Clinical Trial Site Norfolk Virginia 00000
Clinical Trial Site Richmond Virginia 00000
Clinical Trial Site Milwaukee Wisconsin 00000

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05086276, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 20, 2023 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05086276 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →