drugset / Trial / NCT01895972
Long-Term Safety of Latanoprostene Bunod Ophthalmic Solution 0.024% in Japanese Subjects With OAG or OHT
NaSingle-groupOpen-labelTreatment
Summary
The objective of this study is to demonstrate the clinical safety of latanoprostene bunod 0.024% once daily (QD) over a 1-year treatment period.
Timeline
- Start
- 2013-07-05
- Primary completion
- 2015-04-02
- Completion
- 2015-04-14
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Latanoprostene bunod | Small molecule | 0.024 % | Topical |