NCT06309953

A Study to Evaluate Early Treatment Outcomes With Miebo™ in Subjects With Dry Eye Disease

An Open-Label, Multicenter, Phase 4 Study to Evaluate Early Treatment Outcomes With Miebo™ in Subjects With Dry Eye Disease
Bausch & Lomb Incorporated·Phase 4·ClinicalTrials.gov·drugRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Dry Eye
Drug/Device/Intervention
Miebo
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Bausch & Lomb Incorporated
Location
Petaluma,Pittsburg,Stillwater,Kansas City,Brecksville, United States of America
Timeline & enrollment
Phase
Phase 4
Start date
Feb 28, 2024
End date
Jun 28, 2024
Enrollment
100 participants
Primary outcome

Mean change from baseline (CFB) in dry eye symptom severity at Visit 3

Summary

An Open-Label, Multicenter, Phase 4 Study to Evaluate Early Treatment Outcomes With Miebo™ in
 Subjects With Dry Eye Disease

ICD-10 classifications
Ocular painAvulsion of eyeOther corneal deformitiesCorneal ulcerDry mouth, unspecified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06309953
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06309953 through Pure Global AI's free database. This Phase 4 trial is sponsored by Bausch & Lomb Incorporated and is currently Recruiting. The study focuses on Dry Eye. Target enrollment is 100 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.