drugset / Trial / NCT04285580
A Phase 3b Study Evaluating the 24-Hour Intraocular Pressure Lowering Effect of Bimatoprost SR in Patients With Open-Angle Glaucoma or Ocular Hypertension
Non-randomizedParallel-groupOpen-labelTreatment
Summary
This study will evaluate the 24-hour intraocular pressure lowering effect and safety after a single administration of Bimatoprost SR in patients with Open-Angle Glaucoma or Ocular Hypertension
Timeline
- Start
- 2020-06-11
- Primary completion
- 2022-05-14
- Completion
- 2022-05-14
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bimatoprost | Other / unclassified | 10 ug | Intravitreal |
| Subject | Bimatoprost | Other / unclassified | 0.01 % | Topical |