drugset / Trial / NCT02537015
An Open-label Extension Study to Evaluate the Safety of the 13 mg Bimatoprost Ocular Insert
NaSingle-groupOpen-labelTreatment
Summary
This study evaluated the long-term (9-months) safety of the Bimatoprost Ocular Insert in participants with Glaucoma or Ocular Hypertension who completed study FSV5-004. All the participants received Bimatoprost Ocular Insert and wore it for approximately 3 months (12 weeks), then had that Insert removed and a new Insert placed for another 26 weeks (approximately 6 months).
Timeline
- Start
- 2015-08-10
- Primary completion
- 2016-08-11
- Completion
- 2016-08-11
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bimatoprost | Other / unclassified | 13 mg | Other |