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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

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Trial Profile

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

Status: Discontinued
Phase of Trial: Phase II

Latest Information Update: 24 Apr 2023

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At a glance

  • Drugs FX 322 (Primary)
  • Indications Noise-induced hearing loss; Sensorineural hearing loss; Sudden hearing loss
  • Focus Therapeutic Use
  • Sponsors Frequency Therapeutics

    • Most Recent Events

    • 13 Mar 2023 According to a Frequency Therapeutics media release, company announced given the outcome of this study, the Company has undertaken actions to reduce expenses and headcount, these cuts will be completed by the end of April 2023.
    • 10 Mar 2023 Status changed to discontinued, according to a Frequency therapeutic media release.
    • 13 Feb 2023 Primary endpoint (Speech Perception) has not been met, according to a Frequency Therapeutics media release.

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