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A Clinical Trial of YH1177 in Patients With Otitis Media and Otorrhea

Otitis Media Clinical Trial

Official title:
A Randomized, Double-blind, Multicenter, Phase2 Trial to Evaluate the Safety and Efficacy of YH1177 or YH1177-D Otic Soultion in Patients With Otitis Media and Otorrhea

Clinical Trial Summary

In patients with otitis media presenting with otoscopy-confirmed otorrhea who had tympanostomy tube insertion or tympanic perforation, to evaluate the safety, tolerability, and the proportion of patients with cessation of otorrhea after ear-drop administration of YH1177 or YH1177-D for 14 days and therefore to determine the optimal clinical dose.

Clinical Trial Description

Patients with otitis media presenting with otoscopy-confirmed otorrhea who had tympanostomy tube insertion or tympanic perforation. Screening should be completed within 7 days prior to randomization. patients with otitis media presenting with otoscopy-confirmed otorrhea who had tympanostomy tube insertion or tympanic perforation at randomization visit will be randomized in one of the defined groups. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02817347
Study type Interventional
Source Yuhan Corporation
Contact
Status Terminated
Phase Phase 1/Phase 2
Start date June 2016
Completion date April 13, 2017
View Details
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