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
Latest Information Update: 26 May 2022
At a glance
- Drugs FX 322 (Primary)
- Indications Sensorineural hearing loss
- Focus Adverse reactions; Therapeutic Use
- Sponsors Frequency Therapeutics
- 24 May 2022 Status changed from active, no longer recruiting to completed.
- 21 Dec 2021 Status changed from completed to active, no longer recruiting.
- 21 Dec 2021 Planned End Date changed from 1 Jun 2021 to 1 May 2022.