drugset / Trial / NCT06388070
To Evaluate the Efficacy and Safety of HUC3-053 in Patients With Dry Eye Syndrome
RandomizedParallel-groupDouble-blindTreatment
Summary
This is a multi-center, randomized, double-blinded, non-inferiority study to evaluate the efficacy and safety of HUC3-053 in patients with dry eye syndrome. After a 2-week run-in period, patients will be randomized equally to the HUC3-053 or Hyalein Mini Eye Drops administered bilaterally five to six times a day for 12 weeks.
Timeline
- Start
- 2024-05-20
- Primary completion
- 2025-03-14
- Completion
- 2025-03-21
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Hyalein Mini Eye Drops | Unknown | 0.3 % | Other |
| Subject | Hyaluronic Acid | Other / unclassified | 0.3 % | Other |