Trial Search Results

Efficacy and Safety Study of Bimatoprost Sustained-Release (SR) in Participants With Open-angle Glaucoma or Ocular Hypertension

This study will evaluate the efficacy and safety of bimatoprost SR in participants with open-angle glaucoma or ocular hypertension. The study includes a 12-month treatment period with an 8-month extended follow-up.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Allergan

Stanford Investigator(s):

Intervention(s):

  • Drug: Bimatoprost SR
  • Drug: Active Comparator: Timolol 0.5%
  • Other: Sham: Applicator Without Needle
  • Drug: Timolol Vehicle (placebo)

Phase:

Phase 3

Eligibility


Inclusion Criteria:

-Diagnosis of either open-angle glaucoma or ocular hypertension in each eye and both eyes
require IOP-lowering treatment.

Exclusion Criteria:

   - Previous enrollment in another Allergan Bimatoprost SR Study.

   - Eye surgery (including cataract surgery) and/or any eye laser surgery within the past
   6 months in the study eye

   - Anticipated need for laser eye surgery in either eye within the first 52 weeks of the
   study duration

   - History of glaucoma surgery

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Kristina Liu
(408) 726-5119
Recruiting