Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01908764

Pharmacokinetic Study of AL-60371 Otic Suspension in Pediatric Subjects Following Tympanostomy Tube Surgery

An Open-Label, Single Dose, Pharmacokinetic Study of AL-60371 Otic Suspension, 0.3% in Pediatric Subjects Following Tympanostomy Tube Surgery

Status
Withdrawn
Phase
Phase 1
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
6 Months – 12 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to describe the pharmacokinetics of AL-60371 otic suspension following two posologies of bilateral ototopical doses in pediatric subjects immediately after bilateral tympanostomy tube surgery.

Conditions

Interventions

TypeNameDescription
DRUGAL-60371 otic suspension

Timeline

Start date
2014-11-01
Primary completion
2015-01-01
Completion
2015-01-01
First posted
2013-07-26
Last updated
2016-03-08

Source: ClinicalTrials.gov record NCT01908764. Inclusion in this directory is not an endorsement.