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Trials / Completed

CompletedNCT05733624

Clinical Trial to Evaluate the Safety and Efficacy of SCAI-001 Compared to Restasis

A Multicenter, Active Control, Parallel Group, Randomized, Double-blind, Phase II Clinical Trial to Evaluate the Efficacy and Safety of SCAI-001 Eye Drops in Patients With Dry Eye Disease

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
116 (actual)
Sponsor
SCAI Therapeutics · Industry
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

This study is planned to Evaluate the Efficacy and Safety of SCAI-001 Eye Drops(Cyclosporine 0.01%, 0.02%) compared to Restasis(Cyclosporine 0.05%) in Patients with Dry Eye Disease.

Conditions

Interventions

TypeNameDescription
DRUGSCAI-001 0.01% eyedropBID for 12weeks
DRUGSCAI-001 0.02% eyedropBID for 12weeks
DRUGRestasis 0.05% eyedropBID for 12weeks

Timeline

Start date
2023-01-05
Primary completion
2023-08-23
Completion
2024-02-02
First posted
2023-02-17
Last updated
2024-02-05

Locations

11 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT05733624. Inclusion in this directory is not an endorsement.

Clinical Trial to Evaluate the Safety and Efficacy of SCAI-001 Compared to Restasis (NCT05733624) · Clinical Trials Directory