| Not Yet Recruiting | Revive Toric RWE Study Astigmatism | — | 2026-05-01 |
| Not Yet Recruiting | A Study to Evaluate the Use of Topical Ocular BL1332 for the Management of Postoperative Ocular Pain Following Pain, Postoperative | Phase 2 | 2026-04-01 |
| Not Yet Recruiting | A Study to Investigate the Safety and Effectiveness of the Technolas® TENEO 317 Model 2 Excimer Laser for Lase Myopic Astigmatism | N/A | 2026-04-01 |
| Withdrawn | A Study to Assess the Long-Term Safety of Lifitegrast/Perfluorohexyloctane Fixed-Dose Combination in Subjects Dry Eye Disease | Phase 3 | 2025-12-01 |
| Not Yet Recruiting | Effectiveness and Safety of the TENEO 317 Model 2 Excimer Laser to Treat Myopia With or Without Astigmatism by Myopia | N/A | 2025-11-01 |
| Recruiting | Phase 2 Study of BL1107 Eye Drops vs. Timolol in Adults With Primary Open Angle Glaucoma or Ocular Hypertensio Glaucoma | Phase 2 | 2025-10-24 |
| Recruiting | A Study Evaluating the Safety and Efficacy of a Fixed-Dose Combination for Dry Eye Disease Dry Eye Disease | Phase 2 | 2025-10-24 |
| Active Not Recruiting | A Study to Assess Safety, Tolerability, and Pharmacokinetics of Ascending Concentrations of Topical Ocular BL1 Ocular Pain | Phase 1 | 2025-07-29 |
| Completed | A Study to Evaluate Concomitant Perfluorohexyloctane Use With Contact Lens Wear Dry Eye | Phase 4 | 2025-07-02 |
| Completed | A Study Comparing the Efficacy and Safety of Brimonidine Tartrate Ophthalmic Solution 0.025% With Sodium Hyalu Ocular Redness | Phase 3 | 2025-05-22 |
| Completed | A Study to Evaluate Real World Outcomes of the enVista® Aspire (EA) and Aspire Toric (ETA) Intraocular Lens in Cataract | N/A | 2024-08-29 |
| Terminated | Clinical Evaluation of the Performance of the enVista® Aspire™ (EA) Lens Cataract | N/A | 2024-08-15 |
| Active Not Recruiting | Study to Evaluate the Safety and Effectiveness of the enVista® Beyond (EY) EDF Intraocular Lens in Subjects Un Cataract | N/A | 2024-08-07 |
| Active Not Recruiting | A Study to Evaluate Corneal Endothelial Cell Density (ECD) in Subjects With Dry Eye Disease (DED) Administerin Dry Eye | Phase 4 | 2024-07-31 |
| Completed | A Study to Evaluate the enVista® Aspire (EA) Intraocular Lens in Subjects Undergoing Cataract Extraction Cataract | — | 2024-05-30 |
| Completed | A Study to Evaluate the Effect of Miebo™ on Preoperative Biometry/Keratometry and Postoperative Refractive Acc Dry Eye | Phase 4 | 2024-04-30 |
| Recruiting | A Study to Evaluate the Safety and Efficacy of the Bausch + Lomb Myopia Control Lens for the Correction of Myo Myopia | N/A | 2024-03-29 |
| Completed | A Study to Evaluate Early Treatment Outcomes With Miebo™ in Subjects With Dry Eye Disease Dry Eye | Phase 4 | 2024-02-28 |
| Completed | 1-Week Dispensing Evaluation of REVIVE™ Toric Soft Contact Lenses Refractive Ametropia | N/A | 2023-10-04 |
| Recruiting | IC-8 Apthera IOL New Enrollment Post Approval Study Cataract, Presbyopia, Posterior Capsule Opacification | — | 2023-09-08 |
| Completed | Kalifilcon A Toric Compared to Commercially Available Lenses Astigmatism | N/A | 2023-09-05 |
| Completed | Effects of NOV03 on the Tear Film Dry Eye Disease (DED) | Phase 4 | 2023-08-14 |
| Completed | Orientation Characteristics of Daily Disposable Toric Contact Lenses Astigmatism | N/A | 2023-08-11 |
| Completed | Study of Safety and Effectiveness of the Boston Orthokeratology Shaping Lens in the Arise Orthokeratology Lens Myopia | N/A | 2023-07-11 |
| Completed | Evaluation of the Safety and Pharmacokinetics of Brimonidine Tartrate 0.025%/Ketotifen Fumarate 0.035% Combina Allergic Conjunctivitis | Phase 3 | 2023-04-20 |
| Completed | A Study to Evaluate the Safety and Effectiveness of a Contact Lens Cleaning and Disinfecting Solution Refractive Ametropia | N/A | 2023-04-12 |
| Completed | Evaluation of Brimonidine Tartrate/Ketotifen Fumarate Combination in Adults With Seasonal Allergic Conjunctivi Seasonal Allergic Conjunctivitis | Phase 3 | 2022-11-18 |
| Active Not Recruiting | Safety and Effectiveness of the TENEO 317 Model 2 (1.28 US) Excimer Laser for Laser In Situ Keratomileusis (LA Hyperopia | N/A | 2022-11-15 |
| Completed | Evaluation of Product Performance of a New Silicone Hydrogel Multifocal Contact Lens Myopia and Hyperopia and Presbyopia | N/A | 2022-11-07 |
| Completed | Evaluation of Brimonidine Tartrate/Ketotifen Fumarate Combination for the Treatment of Allergic Conjunctivitis Allergic Conjunctivitis | Phase 3 | 2022-10-12 |
| Completed | "Efficacy and Safety of Brimonidine Tartrate Preservative-Free Formulation in Adults With Ocular Redness" Ocular Redness | Phase 3 | 2022-05-13 |
| Withdrawn | A Study to Evaluate the Effect of Latanoprostene Bunod Ophthalmic Solution 0.024% on Episcleral Venous Pressur Ocular Hypertension | Phase 4 | 2022-05-13 |
| Completed | Retrospective Chart Review of enVista Toric 0.9D Intraocular Lenses Corneal Astigmatism | — | 2022-03-08 |
| Completed | 1-Week Dispensing Evaluation of Kalifilcon A Daily Disposable Multifocal Compared to Ultra for Presbyopia Presbyopia | N/A | 2022-02-25 |
| Completed | 1-Week Dispensing Evaluation of Kalifilcon A Toric Contact Lenses Compared to Ultra for Astigmatism Myopia, Astigmatism | N/A | 2022-02-14 |
| Completed | Insertion Clinical Study to Evaluate the Orientation Characteristics of Multiple Kalifilcon A Daily Disposable Astigmatism | N/A | 2021-11-30 |
| Completed | 2-Hour Dispensing Evaluation of Samfilcon A Lenses With EPG01 Packaging Solution Compared to Commercially Avai Contact Lens Wearer | N/A | 2021-09-21 |
| Completed | Biotrue ONEday Contact Lenses With EPG03 Packaging Solution Compared to Biotrue ONEday Contact Lenses Contact Lens Wearer | N/A | 2021-09-15 |
| Completed | Insertion Clinical Study to Evaluate the Aberration Characteristics of Kalifilcon A Toric Lenses Contact Lens Wearer | N/A | 2021-08-25 |
| Completed | Surface Refractive Index Shift and Lens Absorption/Adsorption of Tear Components of Kalifilcon A Lenses vs Dai Habitual Soft Contact Lens Use | N/A | 2021-04-07 |
| Completed | Safety and Efficacy of a New Transepithelial Photorefractive Keratectomy Treatment Ametropia | N/A | 2021-02-02 |
| Completed | Effect of NOV03 on Signs and Symptoms of Dry Eye Disease Associated With Meibomian Gland Dysfunction (Mojave S Dry Eye Disease | Phase 3 | 2020-11-18 |
| Completed | Long-Term Safety and Tolerability of NOV03 (Perfluorohexyloctane) in Subjects Who Completed Trial NVU-003 (Kal Dry Eye Disease (DED) | Phase 3 | 2020-09-24 |
| Completed | Evaluation of Surface Refractive Index Shift of Kalifilcon A Lenses Compared to Dailies Total 1, Precision 1 a Habitual Soft Contact Lens Use | N/A | 2020-09-09 |
| Completed | Evaluation of Visual Acuity of the Envista One-piece Acrylic Toric IOL MX60ET Astigmatism | — | 2020-08-01 |
| Completed | Perfluorohexylcotane (NOV03) for the Treatment of Signs and Symptoms of Dry Eye Disease Associated With Meibom Dry Eye Disease (DED) | Phase 3 | 2020-07-20 |
| Completed | Clinical Study to Evaluate the Safety and Performance of the enVista® One-Piece Hydrophobic Acrylic Trifocal I Cataract | N/A | 2020-03-10 |
| Completed | Safety and Efficacy of Different Add Powers With a New Presbyopic Lasik Treatment Algorithm Ametropia | N/A | 2020-01-26 |
| Completed | A Study of B + L Ophthalmic Viscosurgical Device (OVD) CVisc50 Cataract | N/A | 2019-11-26 |
| Completed | Safety and IOP-Lowering Effects of WB007 Glaucoma, Primary Open Angle, Ocular Hypertension | Phase 1 / Phase 2 | 2019-11-14 |
| Completed | A Safety and Effectiveness Study of a New Preservative Free Rewetting Drop Contact Lens Wear | N/A | 2019-11-07 |
| Completed | Product Performance of a New Silicone Hydrogel Contact Lens Myopia | N/A | 2019-07-31 |
| Completed | A Study With Technolas® TENEO 317 Model 2 Excimer Laser to Treat Participants With Myopia or Myopic Astigmatis Myopia, Myopic Astigmatism | N/A | 2019-07-25 |
| Completed | A Study to Evaluate the Safety and Efficacy of Kalifilcon A Daily Disposable Contact Lens Contact Lens Wear | N/A | 2019-05-31 |
| Completed | A Safety and Effectiveness Study of BL-ABT12 Multi-Purpose Solution for Use by Participants With Soft Contact Contact Lens Wear | N/A | 2019-03-08 |
| Completed | A Study to Evaluate the Safety and Effectiveness of a Silicone Hydrogel Custom Contact Lens When Compared to A Contact Lens Wear | N/A | 2019-02-27 |
| Completed | Evaluate the Safety and Effectiveness of the Biotrue ONEday for Astigmatism Astigmatism | N/A | 2018-10-10 |
| Completed | Evaluate the Safety and Effectiveness of the enVista® One-Piece Hydrophobic Acrylic Trifocal Intraocular Lens Cataract | N/A | 2018-05-31 |
| Completed | Bausch & Lomb Ophthalmic Viscosurgical Device (OVD) Dispersive (DVisc40) Cataract | N/A | 2018-05-09 |
| Completed | A Single-Center Evaluation of the Relative Efficacy of EM-100 Compared to Zaditor® (Ketotifen Fumarate Ophthal Allergic Conjunctivitis | Phase 3 | 2018-04-07 |
| Completed | Therapeutic Equivalence Study of Generic Brinzolamide vs Azopt Glaucoma, Open Angle or Ocular Hypertension | Phase 1 / Phase 2 | 2018-02-28 |
| Completed | Clinical Study of Approved Contact Lenses Myopia | N/A | 2017-10-23 |
| Completed | Corneal Endothelial Cell Density in Eyes Treated With a Fluocinolone Acetonide Intravitreal Implant Uveitis, Posterior | — | 2017-07-14 |
| Completed | Evaluation of the Safety, Systemic Pharmacokinetics, and Tolerability of Single and Repeat Ocular Installation Healthy | Phase 1 | 2017-04-10 |
| Completed | Study to Explore the Pharmacokinetics and Pharmacodynamics of Epinephrine in Healthy Male and Female Subjects Anaphylaxis | Phase 1 | 2017-03-23 |
| Completed | LE Gel for the Treatment of Ocular Inflammation and Pain Following Cataract Surgery Cataract, Pain, Ocular Inflammation | Phase 3 | 2016-06-01 |
| Completed | Evaluation of Corneal Endothelial Cell Density in Subjects Who Have Had a Fluocinolone Acetonide Implant Inflammation, Uveitis | — | 2016-02-04 |
| Completed | A Safety and Effectiveness Study of a New Contact Lens Cleaning and Disinfecting Solution Contact Lens Wear | N/A | 2015-05-31 |
| Completed | Post Approval Study to Evaluate the Trulign™ Toric Posterior Chamber IOL Cataract | — | 2015-03-19 |
| Completed | Study Evaluating the Drug Interaction Potential of Luliconazole Cream 1% in Participants With Tinea Pedis and Tinea Pedis, Tinea Cruris | Phase 4 | 2015-02-03 |
| Completed | Study to Evaluate the Product Performance of a New Silicone Hydrogel Contact Lens Corneal Deformity | N/A | 2014-11-03 |
| Completed | Loteprednol Etabonate Ophthalmic Gel for the Treatment of Ocular Inflammation and Pain Following Cataract Surg Inflammation, Pain, Cataract | Phase 3 | 2014-09-01 |
| Completed | Safety of Brimonidine Tartrate Ophthalmic Solution in a Population of Pediatric, Adult, and Geriatric Particip Hyperemia | Phase 3 | 2014-02-22 |
| Completed | Pharmacokinetics and Safety of Topical Administration of Brimonidine Tartrate Ophthalmic Solution 0.025%. Hyperemia | Phase 1 | 2014-02-01 |
| Completed | Loteprednol Ophthalmic Gel for the Treatment of Ocular Inflammation and Pain Following Cataract Surgery Inflammation, Pain, Cataract | Phase 3 | 2013-12-01 |
| Completed | Efficacy and Safety of Brimonidine Tartrate Ophthalmic Solution in Adult and Geriatric Participants With Ocula Hyperemia | Phase 3 | 2013-11-07 |
| Completed | Long-Term Safety of Latanoprostene Bunod Ophthalmic Solution 0.024% in Japanese Subjects With OAG or OHT Glaucoma, Ocular Hypertension | Phase 3 | 2013-07-05 |
| Completed | Efficacy of Latanoprostene Bunod in Lowering Intraocular Pressure in Japanese Healthy Male Volunteers Intraocular Pressure | Phase 1 | 2013-07-01 |
| Completed | A Study to Evaluate a Mid Add Multi-Focal Soft Contact Lens Presbyopia | N/A | 2013-06-01 |
| Completed | Loteprednol vs Prednisolone for the Treatment of Intraocular Inflammation Following Cataract Surgery in Childr Cataract | Phase 3 | 2013-06-01 |
| Completed | Lotemax® Gel 0.5% and Restasis 0.05% in Participants With Mild or Moderate Keratoconjunctivitis Sicca (Dry Eye Keratoconjunctivitis Sicca | Phase 2 | 2013-05-17 |
| Withdrawn | A Study to Evaluate the Performance and Safety of Artelac Rebalance® Versus Vismed in the Management of Dry Ey Dry Eye | N/A | 2013-05-01 |
| Completed | A Study to Evaluate the Product Performance of a New Silicone Hydrogel Contact Lens Myopia | N/A | 2013-04-01 |
| Completed | Hydrophobic Acrylic Toric IOL Designed to Reduce the Effects of Preoperative Corneal Astigmatism Astigmatism | N/A | 2013-03-06 |
| Completed | Corneal Endothelial Cell Density Changes, When Mapracorat Ophthalmic Suspension 3%, is Administered for 14 Day Corneal Endothelial Cell Changes | Phase 1 | 2013-02-01 |
| Terminated | Clinical and Microbial Efficacy of Besifloxacin Ophthalmic Suspension, 0.6% in the Treatment of Bacterial Conj Bacterial Conjunctivitis | Phase 3 | 2013-02-01 |
| Completed | Comparing Safety and Efficacy of BOL-303259-X With Timolol Maleate in Subjects With Open-Angle Glaucoma or Ocu Open-Angle Glaucoma, Ocular Hypertension | Phase 3 | 2013-01-31 |
| Completed | Comparing the Safety and Efficacy of BOL-303259-X Ophthalmic Solution With Timolol Maleate Ophthalmic Solution Open-Angle Glaucoma, Ocular Hypertension | Phase 3 | 2013-01-01 |
| Completed | Bepotastine Besilate Nasal Sprays in the Treatment of Seasonal Allergic Rhinitis (SAR) Seasonal Allergic Rhinitis | Phase 2 | 2013-01-01 |
| Completed | Tear Fluid Levels of Loteprednol Etabonate Ophthalmic Gel 0.5% Following a Single Instillation Pharmacokinetics | Phase 1 | 2013-01-01 |
| Completed | Evaluation of Clinical Outcomes Following Implantation of a Sub-2mm Hydrophilic MICS Intraocular Lens Cataract | N/A | 2012-11-08 |
| Completed | BOL-303259-X With Timolol 0.5% in Subjects With Open-Angle Glaucoma or Ocular Hypertension Ocular Hypertension, Open Angle Glaucoma | Phase 2 | 2012-11-01 |
| Completed | Mapracorat Ophthalmic Suspension, 3% for the Treatment of Ocular Inflammation and Pain Following Cataract Surg Cataract, Inflammation, Surgery | Phase 3 | 2012-07-01 |
| Completed | Mapracorat Ophthalmic Suspension, 3% for the Treatment of Ocular Inflammation and Pain Following Cataract Surg Cataract, Inflammation, Surgery | Phase 3 | 2012-07-01 |
| Completed | Evaluation of Ocular Comfort With ISTA Tears vs Systane Dry Eye Disease | N/A | 2012-06-01 |
| Completed | A Study to Evaluate the Product Feasibility of Two New Silicone Hydrogel Contact Lenses Myopia | N/A | 2012-04-01 |
| Completed | Therapeutic Equivalence Study of Generic Brinzolamide vs Azopt Glaucoma, Open Angle or Ocular Hypertension | Phase 3 | 2012-01-01 |
| Completed | A Study to Evaluate the Product Performance of a Low Add MultiFocal Soft Contact Lens Presbyopia | N/A | 2012-01-01 |
| Completed | A Study to Evaluate the Feasibility of a High Add Multi Focal Contact Lens Presbyopia | N/A | 2012-01-01 |
| Completed | Bepotastine Besilate-corticosteroid Nasal Spray Combination Compared to Placebo, Bepotastine Besilate Nasal Sp Seasonal Allergic Rhinitis | Phase 2 | 2011-12-01 |
| Completed | A Study to Evaluate the Product Feasibility of a New Silicone Hydrogel Contact Lens Myopia | N/A | 2011-08-01 |
| Completed | A Study to Evaluate the Safety and Efficacy of a New Silicone Hydrogel Contact Lens Design Myopia | N/A | 2011-08-01 |
| Completed | A Study to Evaluate the Product Performance of the PureVision®2 High Definition (HD) Contact Lens Myopia | N/A | 2011-07-01 |
| Completed | Safety and Efficacy of a Contact Lens for Daily Disposable Use Myopia | N/A | 2011-06-01 |
| Terminated | Besifloxacin Ophthalmic Suspension Verses Gatifloxacin Ophthalmic Solution in Neonates With Bacterial Conjunct Bacterial Conjunctivitis | Phase 3 | 2011-05-01 |
| Completed | Efficacy of Bromfenac Ophthalmic Solution in Patients Undergoing Cataract Surgery Pain, Inflammation, Cataract | Phase 3 | 2011-05-01 |
| Completed | A Study to Evaluate a Modified Contact Lens Myopia | N/A | 2011-04-01 |
| Terminated | Twelve Month Clinical Evaluation of KeraSoft IC Soft Contact Lenses Keratoconus | N/A | 2011-04-01 |
| Terminated | Tear Evaluation Between Habitual Contact Lens Wearers and Non Contact Lens Wearers Dry Eye | — | 2011-02-01 |
| Terminated | Mapracorat Ophthalmic Suspension, 3% for the Treatment of Ocular Inflammation Following Cataract Surgery Inflammation, Pain, Cataract | Phase 3 | 2011-02-01 |
| Completed | Mapracorat Ophthalmic Formulation in Subjects With Allergic Conjunctivitis Conjunctivitis, Allergic | Phase 2 | 2011-02-01 |
| Completed | Evaluation of Two Daily Disposable Contact Lenses. Myopia | N/A | 2011-01-01 |
| Completed | Study Comparing the Safety and Efficacy of BOL-303259-X to Latanoprost in Subjects With Glaucoma or Ocular Hyp Intraocular Pressure | Phase 2 | 2010-12-13 |
| Completed | Evaluation of the Feasibility a New Silicone Hydrogel Contact Lens Myopia | N/A | 2010-12-01 |
| Completed | Safety and Efficacy of Bepotastine Besilate Nasal Spray in the Treatment of Seasonal Allergic Rhinitis Seasonal Allergic Rhinitis | Phase 2 | 2010-12-01 |
| Completed | A Study to Evaluate the Performance of Two Designs of Soft Toric Lenses Myopia | N/A | 2010-12-01 |
| Completed | Evaluation of a New Silicone Hydrogel Contact Lens Myopia | N/A | 2010-12-01 |
| Completed | A Study to Evaluate a New Silicone Hydrogel Contact Lens Myopia | N/A | 2010-12-01 |
| Completed | Mapracorat Ophthalmic Suspension for the Treatment of Ocular Inflammation Following Cataract Surgery Cataract | Phase 3 | 2010-11-01 |
| Completed | Product Feasibility of a New Silicone Hydrogel Contact Lens Myopia | N/A | 2010-11-01 |
| Completed | Study of A New Contact Lens Cleaning and Disinfecting Solution Vision Disorders | N/A | 2010-11-01 |
| Completed | One-Piece Hydrophobic Acrylic Intraocular Lens in Subjects Undergoing Cataract Extraction Aphakia, Cataract | Phase 3 | 2010-10-01 |
| Completed | Study to Evaluate a Contact Lens Lubricating and Rewetting Drop Dry Eye | N/A | 2010-10-01 |
| Terminated | Accommodation Measurements After Bilateral Implantation of an Aspheric Accommodating Lens and Monofocal Aspher Cataract | Phase 4 | 2010-10-01 |
| Completed | A Dose Ranging Study to Evaluate Safety and Efficacy of Bromfenac Ophthalmic Solution in Dry Eye Disease Dry Eye Syndrome | Phase 3 | 2010-09-01 |
| Completed | A Study to Evaluate the Safety and Efficacy of Lotemax Ophthalmic Suspension 0.5% Conjunctivitis, Seasonal Allergic, Conjunctivitis, Giant Papillary, Inflammation | Phase 4 | 2010-08-05 |
| Completed | Alrex® Versus Patanol in the Treatment of Seasonal Allergic Conjunctivitis(SAC) Seasonal Allergic Conjunctivitis | Phase 3 | 2010-08-01 |
| Completed | A Study to Evaluate the Product Performance of a Daily Disposable Contact Lens Myopia, Contact Lenses | N/A | 2010-08-01 |
| Completed | Product Performance of a Daily Disposable Contact Lens Myopia | N/A | 2010-08-01 |
| Completed | Three Intraocular Lenses Designed to Improve Distance, Intermediate and Near Vision Following Lens Extraction Cataract | Phase 4 | 2010-07-01 |
| Completed | Study Evaluating the Safety of KetoNaph Ophthalmic Solution in Healthy Volunteers Allergic Conjunctivitis | Phase 3 | 2010-07-01 |
| Completed | Study to Assess the Safety and Efficacy of BOL-303242-X Ophthalmic Suspension in Dry Eye Syndrome Dry Eye Syndrome | Phase 2 | 2010-07-01 |
| Completed | Safety and Efficacy of Bepotastine Besilate Ophthalmic Solution in Seasonal Allergic Conjunctivitis Patients Allergic Conjunctivitis | Phase 2 | 2010-06-01 |
| Completed | Toric Intraocular Lens Following Cataract Surgery Cataract, Astigmatism | N/A | 2010-06-01 |
| Completed | Evaluation of 3 Intraocular Lenses Following Lens Extraction Cataract | Phase 4 | 2010-06-01 |
| Completed | Safety of Besivance™ (Besifloxacin Ophthalmic Suspension) 0.6% Compared to Vehicle Bacterial Conjunctivitis | Phase 3 | 2010-06-01 |
| Completed | Feasibility of a New Silicone Hydrogel Lens Myopia | N/A | 2010-05-01 |
| Completed | Safety, Pharmacokinetics, and Efficacy of Bepotastine Besilate Nasal Product After Ragweed Pollen Exposure in Seasonal Allergic Rhinitis | Phase 1 / Phase 2 | 2010-05-01 |
| Completed | Evaluation of Two Different Designs of Bausch & Lomb Contact Lenses Myopia | N/A | 2010-05-01 |
| Completed | Extension Study to Gather Data on Effect of Macugen on the Corneal Endothelium Age-Related Macular Degeneration, Retinal Vein Occlusion, Diabetic Macular Edema | Phase 4 | 2010-04-22 |
| Completed | A Study to Assess the Safety and Efficacy of a Daily Disposable Contact Lens Myopia | N/A | 2010-04-01 |
| Completed | Loteprednol Ophthalmic Base Compared to Loteprednol Ophthalmic Suspension vs Placebo in an Allergen Challenge Allergic Conjunctivitis | Phase 2 | 2010-04-01 |
| Completed | Ketotifen/Naphazoline Ophthalmic Solution in the Conjunctival Allergen Challenge Model of Acute Allergic Conju Allergic Conjunctivitis | Phase 3 | 2010-02-01 |
| Completed | Evaluation of Loteprednol Etabonate Versus Vehicle for the Treatment of Inflammation and Pain Following Catara Inflammation, Pain | Phase 3 | 2010-02-01 |
| Completed | Loteprednol Etabonate Versus Vehicle for the Treatment of Inflammation and Pain Following Cataract Surgery Inflammation, Pain | Phase 3 | 2009-11-01 |
| Completed | A Study to Evaluate the Clinical Performance of a Novel Multipurpose Solution Ocular Discomfort | N/A | 2009-11-01 |
| Completed | Loteprednol and Tobramycin Versus Tobramycin and Dexamethasone, in the Treatment of Blepharokeratoconjunctivit Conjunctivitis, Keratitis, Blepharitis | Phase 3 | 2009-10-01 |
| Completed | Efficacy of Besifloxacin Ophthalmic Suspension in the Treatment of Bacterial Conjunctivitis Bacterial Conjunctivitis | Phase 2 / Phase 3 | 2009-10-01 |
| Completed | Performance Evaluation of Contact Lenses Among a Population of Adapted Contact Lens Wearers Vision Disorders | N/A | 2009-09-01 |
| Completed | Co-Axial Micro-Incision Versus Co-Axial Small Incision Cataract Surgery Using the Stellaris Enhancement System Cataract, Aphakia | Phase 4 | 2009-08-01 |
| Completed | Evaluation of BOL-303242-X Versus Vehicle for the Treatment of Inflammation Following Cataract Surgery Cataract, Inflammation | Phase 2 | 2009-06-01 |
| Completed | Concentration of Besifloxacin, Gatifloxacin, and Moxifloxacin in Human Conjunctiva After Topical Instillation Healthy | Phase 1 | 2009-03-01 |
| Completed | Study of T-PRED(TM) Compared to Pred Forte(R) II Cataract | Phase 3 | 2009-02-01 |
| Completed | Assessment of the Concentrations of Besifloxacin, Moxifloxacin, or Gatifloxacin in the Aqueous Humor of Subjec Cataract Extraction | Phase 1 | 2009-02-01 |
| Completed | Efficacy Study of Bromfenac Ophthalmic Solution in Patients Undergoing Cataract Surgery Pain, Inflammation | Phase 3 | 2009-02-01 |
| Completed | Safety and Effectiveness of the Akreos Toric Intraocular Lens. Cataract, Astigmatism | Phase 4 | 2009-02-01 |
| Terminated | Evaluation of the Safety and Effectiveness of the Akreos MI Five-0 Intraocular Lens. Cataract | N/A | 2008-11-01 |
| Completed | A Product Performance Evaluation of a Novel Contact Lens for Daily Disposable Use Myopia | N/A | 2008-11-01 |
| Completed | Ketotifen/Naphazoline Ophthalmic Solution in the Conjunctival Allergen Challenge Model of Allergic Conjunctivi Allergic Conjunctivitis | Phase 3 | 2008-10-01 |
| Completed | One-Day Dispensing Clinical Evaluation of SofLens Daily Disposable Lenses Compared to a Marketed 1 Day Contact Myopia | N/A | 2008-10-01 |
| Completed | Comparative Study of the Wearing Satisfaction of Two Soft Contact Lens Designs. Myopia | N/A | 2008-09-01 |
| Completed | Safety and Efficacy of an Ophthalmic Solution in Dry Eye Disease Dry Eye Disease | Phase 2 | 2008-08-13 |
| Completed | Technolas 217z Laser With Zyoptix Aspheric Algorithm Used for the LASIK Treatment of Myopia and Myopic Astigma Myopia, Astigmatism | N/A | 2008-08-01 |
| Completed | Evaluation of a Multi-Purpose Solution Contact Lens Solutions | N/A | 2008-07-01 |
| Completed | Ocular Responses to Short and Long-term Lens Wear Ametropia | N/A | 2008-07-01 |
| Completed | Loteprednol Etabonate in an Ophthalmic Base vs Vehicle for the Treatment of Inflammation Following Cataract Su Ocular Inflammation | Phase 3 | 2008-06-01 |
| Completed | Efficacy and Safety of Bromfenac Ophthalmic Solution in Cataract Surgery Cataract | Phase 3 | 2008-06-01 |
| Completed | Safety and Efficacy of Zylet vs Lotemax, Tobramycin and Vehicle in Pediatric Blepharoconjunctivitis Conjunctivitis | Phase 4 | 2008-06-01 |
| Completed | Efficacy and Safety of Bromfenac Ophthalmic Solution in Cataract Surgery Cataract | Phase 3 | 2008-06-01 |
| Completed | Study of T-PRED(TM) Compared to Pred Forte(R) Cataract | Phase 2 | 2008-05-01 |
| Completed | Indomethacin Eyedrops Compared With Ketorolac Eyedrops for Ocular Inflammation Following Cataract Surgery Cataract, Inflammation | Phase 4 | 2008-04-01 |
| Completed | Product Performance of a Toric Contact Lens Myopia, Astigmatism | N/A | 2008-04-01 |
| Completed | Efficacy Study of Ecabet Ophthalmic Solution in Dry Eye Disease Dry Eye Disease | Phase 2 | 2008-03-22 |
| Completed | Safety and Efficacy of a Bausch & Lomb Multipurpose Solution When Compared to Ciba Vision Aquify Multipurpose Contact Lens Solutions | N/A | 2008-03-01 |
| Completed | Loteprednol Etabonate Ophthalmic Ointment vs. Vehicle in the Treatment of Inflammation Following Cataract Surg Ocular Inflammation | Phase 3 | 2008-03-01 |
| Completed | Performance of Bausch & Lomb ReNu MultiPlus Multi-Purpose Solution in a New Packaging Configuration Comfort | N/A | 2008-03-01 |
| Completed | Comparative Performance of a Bausch & Lomb Multipurpose Solution and Alcon OptiFree Replenish Multipurpose Sol Adverse Effect of Contact Lens Solution | N/A | 2008-02-01 |
| Completed | Comparative Performance of PureVision, Acuvue Oasys and O2Optix Myopia | Phase 4 | 2008-02-01 |
| Completed | A Phase 2, Dose Finding Study of PF-03187207 in Patients With Primary Open Angle Glaucoma or Ocular Hypertensi Primary Open Angle Glaucoma, Ocular Hypertension | Phase 2 | 2007-12-01 |
| Completed | Comparative Performance of PureVision Lens Designs Myopia | Phase 3 | 2007-12-01 |
| Completed | Efficacy and Safety Study of Bepotastine Besilate Ophthalmic Solution in Allergic Conjunctivitis Allergic Conjunctivitis | Phase 3 | 2007-10-01 |
| Completed | Efficacy and Safety of Bromfenac Ophthalmic Solution Cataract Surgery | Phase 2 | 2007-10-01 |
| Completed | Safety Study for Bepotastine Besilate Ophthalmic Solution in Normal Volunteers Allergic Conjunctivitis | Phase 3 | 2007-10-01 |
| Completed | Corneal Endothelial Cell Density Changes In Healthy Subjects, When Administered ISV-403 for 5 Days Healthy | Phase 1 | 2007-05-01 |
| Completed | Dose-Finding Study Comparing the Safety and Efficacy of Latanoprost to a Novel Treatment for Glaucoma Primary Open Angle Glaucoma, Ocular Hypertension, Pigmentary Glaucoma | Phase 2 | 2007-03-01 |
| Completed | Evaluation of the Onset and Duration of Action of Bepotastine Besilate Ophthalmic Solution in Acute Allergic C Conjunctivitis, Allergic | Phase 2 / Phase 3 | 2007-02-01 |
| Completed | Zylet vs TobraDex in Blepharokeratoconjunctivitis Blepharokeratoconjunctivitis | Phase 4 | 2007-01-01 |
| Completed | Efficacy and Safety of Topical Bromfenac Ophthalmic Solution vs. Placebo in Subjects With Allergic Conjunctivi Allergic Conjunctivitis | Phase 3 | 2006-11-01 |
| Completed | Pediatric Zylet Safety and Efficacy Study Chalazion, Hordeolum | Phase 4 | 2006-11-01 |
| Completed | Systemic Pharmacokinetics of BOL-303224-A Conjunctivitis, Bacterial | Phase 1 | 2006-10-01 |
| Terminated | A Study to Evaluate Plasmin for the Creation of a Posterior Vitreous Detachment (PVD) Vitreoretinal Traction Syndrome | Phase 1 / Phase 2 | 2006-09-01 |
| Completed | Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome Dry Eye Syndromes | Phase 2 | 2006-09-01 |
| Completed | Evaluation of the Safety & Effectiveness of the Bausch & Lomb AKREOS® TL Intraocular Lens Cataract, Aphakia | Phase 4 | 2006-09-01 |
| Completed | A Study to Determine if 0.6% ISV-403 is Safe and Effective in the Treatment of Bacterial Conjunctivitis. Acute Bacterial Conjunctivitis | Phase 3 | 2006-06-01 |
| Completed | A Study to Investigate the Safety and Efficacy of BOL-303224 in the Treatment of Bacterial Conjunctivitis Acute Bacterial Conjunctivitis | Phase 3 | 2006-06-01 |
| Completed | Safety/Efficacy of Bromfenac Ophthalmic Solution for Ocular Inflammation and Pain Associated With Cataract Sur Pain, Inflammation | Phase 3 | 2006-06-01 |
| Terminated | Study to Evaluate Plasmin for the Creation of a Posterior Vitreous Detachment Vitreoretinal Traction Syndrome | Phase 2 | 2006-04-01 |
| Completed | Loteprednol Etabonate Opthalmic Suspension for the Treatment of Dry Eye Dry Eye | Phase 2 | 2005-11-01 |
| Completed | A Study to Investigate the Safety and Effectiveness of Aspheric Laser Refractive Surgery Treatments for Myopia Myopia, Astigmatism | N/A | 2005-10-01 |
| Completed | A Clinical Evaluation of the Next Generation Diagnostic Instrument (NGDI) Healthy | N/A | 2005-08-01 |
| Completed | Assessment of Intravitreous Injections of Vitrase for Inducing Posterior Vitreous Detachment Vitreous Detachment, Diabetic Retinopathy | Phase 2 | 2005-07-01 |
| Completed | A Bioequivalence Study of Tobramycin and Prednisolone Acetate Compared to PredForte Eye Infections, Postoperative Complications | Phase 3 | 2005-07-01 |
| Completed | A Study to Evaluate the Safety and Effectiveness of the Technols 217z Zyoptix System for Hyperopia Hyperopia, Astigmatism | N/A | 2005-06-01 |
| Completed | Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome Dry Eye Syndromes | Phase 2 / Phase 3 | 2005-04-01 |
| Completed | Ocular Tolerance and Intraocular Pressure (IOP) Effects of Zylet Versus Tobradex Inflammation | Phase 4 | 2005-02-01 |
| Completed | Clinical and Microbial Efficacy of ISV403 in Bacterial Conjunctivitis Bacterial Conjunctivitis | Phase 2 | 2004-12-01 |
| Completed | Evaluation of Vitrase as a Spreading Agent Pain | Phase 3 | 2004-10-01 |
| Completed | Evaluation of Vitrase as an Adjuvant to Increase Absorption and Dispersion of Other Injected Anesthetics Pain | Phase 4 | 2004-09-01 |
| Completed | Hypersensitivity Reaction to Vitrase (Ovine Hyaluronidase) Drug Hypersensitivity | Phase 1 | 2004-07-01 |
| Completed | Hypersensitivity Reaction to Vitrase (Ovine Hyaluronidase) Drug Hypersensitivity | Phase 1 | 2004-03-01 |
| Completed | Clinical Evaluation of a New Aspheric Intraocular Lens. Cataract | Phase 4 | 2004-01-01 |
| Completed | Safety and Efficacy Study of Topical Bromfenac Versus Placebo to Treat Ocular Inflammation After Cataract Surg Postoperative Complications, Cataract | Phase 3 | 2003-05-01 |
| Completed | Safety and Efficacy of Intravitreal Fluocinolone Acetonide Implants in Patients With Diabetic Macular Edema Diabetic Macular Edema | Phase 2 | 2003-03-01 |
| Terminated | Safety and Efficacy of Fluocinolone Acetonide Intravitreal Implant Non-infectious Uveitis | Phase 2 / Phase 3 | 2002-05-01 |
| Completed | Safety and Efficacy of Fluocinolone Acetonide Intravitreal Implant vs Standardized Therapy Non-infectious Uveitis | Phase 2 / Phase 3 | 2002-04-01 |
| Completed | Efficacy of Fluocinolone Acetonide Intravitreal Implant in Diabetic Macular Edema Diabetic Macular Edema | Phase 2 / Phase 3 | 2001-09-01 |
| Completed | Safety and Efficacy of Fluocinolone Acetonide Intravitreal Implants Noninfectious Posterior Uveitis | Phase 2 / Phase 3 | 2000-12-01 |
| Completed | Safety and Efficacy Study of Vitrase for Clearance of Severe Vitreous Hemorrhage Vitreous Hemorrhage, Diabetic Retinopathy | Phase 3 | 1999-06-01 |
| Completed | Safety and Efficacy Study of Vitrase for Clearance of Severe Vitreous Hemorrhage Vitreous Hemorrhage, Diabetic Retinopathy | Phase 3 | 1998-11-01 |
| Withdrawn | A Study to Evaluate the Safety and Effectiveness of the 217z Laser With Zyoptix for Lasik Myopia, Astigmatism | N/A | — |
| Withdrawn | A Study Of The Safety And Effectiveness Of A New Treatment For Allergic Conjunctivitis Allergic Conjunctivitis | Phase 2 | — |