Evaluation of Safety and Efficacy of Brimonidine Tartrate Ophthalmic Suspension
| Status: | Recruiting |
|---|---|
| Conditions: | High Blood Pressure (Hypertension), Ocular |
| Therapuetic Areas: | Cardiology / Vascular Diseases, Ophthalmology |
| Healthy: | No |
| Age Range: | 2 - Any |
| Updated: | 2/28/2019 |
| Start Date: | September 13, 2018 |
| End Date: | October 2019 |
| Contact: | Sun Pharma Advanced Research Company Limited |
| Email: | clinical.trials@sparcmail.com |
| Phone: | +1 (609) 720-5333 |
A Randomized, Multi-Center, Investigator-Masked, Parallel Group, Equivalence Study of Once Daily Brimonidine Tartrate Ophthalmic Suspension Compared With Three Times Daily ALPHAGAN-P® in Subjects With Open Angle Glaucoma, or Ocular Hypertension
The study will be conducted to evaluate the efficacy and safety of topical administration of
brimonidine tartrate ophthalmic suspension compared with brimonidine tartrate ophthalmic
solution.
brimonidine tartrate ophthalmic suspension compared with brimonidine tartrate ophthalmic
solution.
Inclusion Criteria:
1. Be male or female, of 2 years of age or older
2. Have open-angle glaucoma or ocular hypertension in both the eyes
3. Be able and willing to follow study instructions and complete all required visits.
Exclusion Criteria:
1. Females who are pregnant/lactating.
2. Have uncontrolled systemic disease which might interfere with the study
3. Any known allergy or sensitivity to the study medications or their components
4. Any other clinically relevant abnormality
We found this trial at
27
sites
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