Viewing Study NCT03918109



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Last Modification Date: 2024-10-26 @ 1:08 PM
Study NCT ID: NCT03918109
Status: COMPLETED
Last Update Posted: 2022-12-23
First Post: 2019-04-15

Brief Title: OTO-313 in Subjects With Subjective Tinnitus
Sponsor: Otonomy Inc
Organization: Otonomy Inc

Study Overview

Official Title: A Randomized Double-blind Placebo-controlled Phase 12 Study of OTO-313 Given as a Single Intratympanic Injection in Subjects With Subjective Tinnitus
Status: COMPLETED
Status Verified Date: 2022-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to evaluate the safety tolerability plasma pharmacokinetics PK and exploratory efficacy of OTO-313 administered as an intratympanic injection for the treatment of subjective tinnitus
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None