drugset / Trial / NCT02143843
An Open-Label Extension Study to Evaluate the Safety of the ForSight VISION5 Product
NaSingle-groupOpen-labelTreatment
Summary
This study evaluates the long-term (13-months) safety of the Bimatoprost Ocular Insert in participants with Glaucoma or Ocular Hypertension who completed study FSV5-002. All participants received Bimatoprost Ocular Insert and wore it for approximately 7 months, then had the Insert removed and a new insert placed for another 6 months.
Timeline
- Start
- 2014-06-05
- Primary completion
- 2015-12-31
- Completion
- 2016-01-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bimatoprost | Other / unclassified | 13 mg | — |