deltatrials
Terminated PHASE1 INTERVENTIONAL 4-arm NCT05664100

First in Human Safety Study of FX-345 in Adults With Sensorineural Hearing Loss

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

Sponsor: Frequency Therapeutics

Interventions FX-345 Placebo
Updated 5 times since 2023 Last updated: Apr 25, 2023 Started: Dec 15, 2022 Primary completion: Apr 12, 2023 Completion: Apr 12, 2023
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Terminated

Business reasons

A PHASE1 clinical study on Hearing Loss, Sensorineural, this trial is terminated or withdrawn. The trial is conducted by Frequency Therapeutics and has accumulated 5 data snapshots since 2022. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

~Jan 2023 – ~Mar 2023 · 59 days · monthly snapshot~Mar 2023 – ~May 2023 · 2 months · monthly snapshot~May 2023 – ~Jul 2024 · 14 months · monthly snapshotTerminated~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshot~Sep 2024 – present · 24 months · monthly snapshotTerminated

Change History

5 versions recorded
  1. Sep 2024 — Present [monthly]

    Terminated PHASE1

  2. Jul 2024 — Sep 2024 [monthly]

    Terminated PHASE1

  3. May 2023 — Jul 2024 [monthly]

    Terminated PHASE1

    Status: Active Not RecruitingTerminated

  4. Mar 2023 — May 2023 [monthly]

    Active Not Recruiting PHASE1

    Status: RecruitingActive Not Recruiting

  5. Jan 2023 — Mar 2023 [monthly]

    Recruiting PHASE1

    First recorded

Dec 2022

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Frequency Therapeutics
Data source: Frequency Therapeutics

For direct contact, visit the study record on ClinicalTrials.gov .