Study of OTO-104 in Subjects With Unilateral Meniere's Disease

Last updated: December 19, 2022
Sponsor: Otonomy, Inc.
Overall Status: Completed

Phase

3

Condition

Vestibular Hypofunction

Hearing Loss

Hearing Impairment

Treatment

N/A

Clinical Study ID

NCT02612337
104-201506
  • Ages 18-85
  • All Genders

Study Summary

The purpose of this study is to evaluate the effectiveness of OTO-104 for the treatment of Meniere's disease.

Eligibility Criteria

Inclusion

Inclusion Criteria includes, but is not limited to:

  • Subject has a diagnosis of unilateral Meniere's disease by 1995 American Academy of Otolaryngology - Head and Neck Surgery (AAOHNS) criteria and reports active vertigo for the 2 months prior to the study lead-in period.

  • Subject has experienced active vertigo during the lead-in period.

  • Subject has documented asymmetric sensorineural hearing loss.

  • Subject agrees to maintain their current treatments for Meniere's disease while on-study.

Exclusion Criteria includes, but is not limited to:

  • Subject is pregnant or lactating.

  • Subject has a history of immunodeficiency disease.

  • Subject has a history of previous endolymphatic sac surgery.

  • Subject has a history of previous use of intratympanic (IT) gentamicin in the affected ear.

  • Subject has a history of tympanostomy tubes with evidence of perforation or lack of closure.

  • Subject has experienced an adverse reaction to IT injection of steroids.

  • Subject has used an investigational drug or device in the 3 months prior to screening.

  • Subject has previously been randomized to a trial of OTO-104.

Study Design

Total Participants: 166
Study Start date:
October 27, 2015
Estimated Completion Date:
July 18, 2017

Connect with a study center

  • Many sites in US. Refer to the contact info listed below.

    San Diego, California
    United States

    Site Not Available

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