24-Month Phase I/II Clinical Trial of Bimatoprost Sustained-Release Implant (Bimatoprost SR) in Glaucoma Patients.
E Randy CravenThomas WaltersWilliam C ChristieDouglas G DayRichard A LewisMargot L GoodkinMichelle ChenVeronica WangsadipuraMichael R RobinsonMarina Bejaniannull nullPublished in: Drugs (2020)
Bimatoprost SR showed favorable efficacy and safety profiles up to 24 months, with all evaluated dose strengths demonstrating overall IOP-reducing effects comparable to those of topical bimatoprost. Targeted and sustained delivery of bimatoprost resulted in protracted IOP lowering, suggesting that Bimatoprost SR may represent a transformational new approach to glaucoma therapy. Clinicaltrials.gov identifier: NCT01157364.