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A Three-part, Multicenter, Open Label, Single Dose Study to Assess the Safety, Tolerability, and Efficacy of Intra Labyrinthine (IL) CGF166 in Patients With Severe-to-profound Hearing Loss

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Trial Profile

A Three-part, Multicenter, Open Label, Single Dose Study to Assess the Safety, Tolerability, and Efficacy of Intra Labyrinthine (IL) CGF166 in Patients With Severe-to-profound Hearing Loss

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 31 Mar 2021

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At a glance

  • Drugs CGF 166 (Primary)
  • Indications Hearing loss
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors Novartis Pharmaceuticals

    • Most Recent Events

    • 18 Mar 2020 Status changed from active, no longer recruiting to completed.
    • 14 Nov 2019 Planned End Date changed from 9 Oct 2019 to 5 Dec 2019.
    • 14 Nov 2019 Planned primary completion date changed from 9 Oct 2019 to 4 Dec 2019.

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