Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A Phase 1b, Prospective, Randomized, Single-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Safety of FX-345 Administered as a Single Intratympanic Injection in Adults With Acquired Adult-Onset Sensorineural Hearing Loss

Trial Profile

A Phase 1b, Prospective, Randomized, Single-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Safety of FX-345 Administered as a Single Intratympanic Injection in Adults With Acquired Adult-Onset Sensorineural Hearing Loss

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 03 May 2023

Price :
$35 *
Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs FX 345 (Primary)
  • Indications Sensorineural hearing loss
  • Focus Adverse reactions; First in man; Pharmacokinetics
  • Sponsors Frequency Therapeutics

Most Recent Events

  • 10 Mar 2023 Status changed to discontinued, according to a Frequency Therapeutics media release.
  • 20 Feb 2023 Status changed from recruiting to active, no longer recruiting.
  • 14 Feb 2023 According to a Frequency Therapeutics media release, dosing of FX-345 has been completed in the initial safety cohort in this ongoing trial but the development of FX-345 will be discontinued.

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top