NCT07238699

An Evaluation of the Safety and Tolerability of Ocular Lubricants

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 148 (estimated)
• Sponsor: Alcon Research · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to evaluate the safety and tolerability of two new artificial tear formulations in subjects with moderate dry eye disease.

Detailed description

Each subject will receive 2 investigational products (one drop per eye of each investigational product) in a cross-over study design according to a randomization schedule. Individual duration of participation will be approximately 21 days.

Conditions

• Dry Eye Disease

Interventions

Type	Name	Description
OTHER	FID123440 test formulation	Investigational product
OTHER	FID123437 test formulation	Investigational product
OTHER	FID123440 test formulation	Investigational product

Timeline

• Start date: 2026-03-04
• Primary completion: 2026-08-01
• Completion: 2026-08-01
• First posted: 2025-11-20
• Last updated: 2026-03-11

Locations

4 sites across 1 country: Australia