Bausch & Lomb Incorporated

174 total trials 3 currently recruiting 158 completed

Bausch & Lomb Incorporated sponsors 174 registered US clinical trials on ClinicalTrials.gov, 3 of them currently recruiting, and 158 completed. 60 of these trials are in Phase 3-4 (later-stage) and 42 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Myopia, with 9 trials.

Trial Pipeline

174 total, page 2 of 4

COMPLETED NA

Clinical Study of Approved Contact Lenses

NCT03351101

COMPLETED

Corneal Endothelial Cell Density in Eyes Treated With a Fluocinolone Acetonide Intravitreal Implant

NCT03145025

COMPLETED Phase 1

Evaluation of the Safety, Systemic Pharmacokinetics, and Tolerability of Single and Repeat Ocular Installations

NCT03098953

COMPLETED Phase 3

LE Gel for the Treatment of Ocular Inflammation and Pain Following Cataract Surgery

NCT02786901

COMPLETED

Evaluation of Corneal Endothelial Cell Density in Subjects Who Have Had a Fluocinolone Acetonide Implant

NCT01060787

COMPLETED NA

A Safety and Effectiveness Study of a New Contact Lens Cleaning and Disinfecting Solution

NCT02701556

COMPLETED

Post Approval Study to Evaluate the Trulign™ Toric Posterior Chamber IOL

NCT02394379

COMPLETED Phase 4

Study Evaluating the Drug Interaction Potential of Luliconazole Cream 1% in Participants With Tinea Pedis and Tinea Cruris

NCT02394340

COMPLETED NA

Study to Evaluate the Product Performance of a New Silicone Hydrogel Contact Lens

NCT02258139

COMPLETED Phase 3

Loteprednol Etabonate Ophthalmic Gel for the Treatment of Ocular Inflammation and Pain Following Cataract Surgery

NCT02208297

COMPLETED Phase 3

Safety of Brimonidine Tartrate Ophthalmic Solution in a Population of Pediatric, Adult, and Geriatric Participants

NCT01959243

COMPLETED Phase 1

Pharmacokinetics and Safety of Topical Administration of Brimonidine Tartrate Ophthalmic Solution 0.025%.

NCT02039765

COMPLETED Phase 3

Loteprednol Ophthalmic Gel for the Treatment of Ocular Inflammation and Pain Following Cataract Surgery

NCT01996839

COMPLETED Phase 3

Efficacy and Safety of Brimonidine Tartrate Ophthalmic Solution in Adult and Geriatric Participants With Ocular Redness

NCT01959230

COMPLETED Phase 3

Long-Term Safety of Latanoprostene Bunod Ophthalmic Solution 0.024% in Japanese Subjects With OAG or OHT

NCT01895972

COMPLETED Phase 1

Efficacy of Latanoprostene Bunod in Lowering Intraocular Pressure in Japanese Healthy Male Volunteers

NCT01895985

COMPLETED NA

A Study to Evaluate a Mid Add Multi-Focal Soft Contact Lens

NCT01959178

COMPLETED Phase 3

Loteprednol vs Prednisolone for the Treatment of Intraocular Inflammation Following Cataract Surgery in Children.

NCT01475643

COMPLETED Phase 2

Lotemax® Gel 0.5% and Restasis 0.05% in Participants With Mild or Moderate Keratoconjunctivitis Sicca (Dry Eye Disease)

NCT01817582

COMPLETED NA

A Study to Evaluate the Product Performance of a New Silicone Hydrogel Contact Lens

NCT01873846

COMPLETED NA

Hydrophobic Acrylic Toric IOL Designed to Reduce the Effects of Preoperative Corneal Astigmatism

NCT01852084

COMPLETED Phase 1

Corneal Endothelial Cell Density Changes, When Mapracorat Ophthalmic Suspension 3%, is Administered for 14 Days

NCT01736462

TERMINATED Phase 3

Clinical and Microbial Efficacy of Besifloxacin Ophthalmic Suspension, 0.6% in the Treatment of Bacterial Conjunctivitis

NCT01740388

COMPLETED Phase 3

Comparing Safety and Efficacy of BOL-303259-X With Timolol Maleate in Subjects With Open-Angle Glaucoma or Ocular Hypertension

NCT01749904

COMPLETED Phase 3

Comparing the Safety and Efficacy of BOL-303259-X Ophthalmic Solution With Timolol Maleate Ophthalmic Solution in Subjects With Open-Angle Glaucoma or Ocular Hypertension

NCT01749930

COMPLETED Phase 2

Bepotastine Besilate Nasal Sprays in the Treatment of Seasonal Allergic Rhinitis (SAR)

NCT01753739

COMPLETED Phase 1

Tear Fluid Levels of Loteprednol Etabonate Ophthalmic Gel 0.5% Following a Single Instillation

NCT01736527

COMPLETED Phase 2

BOL-303259-X With Timolol 0.5% in Subjects With Open-Angle Glaucoma or Ocular Hypertension

NCT01707381

COMPLETED Phase 3

Mapracorat Ophthalmic Suspension, 3% for the Treatment of Ocular Inflammation and Pain Following Cataract Surgery

NCT01591161

COMPLETED Phase 3

Mapracorat Ophthalmic Suspension, 3% for the Treatment of Ocular Inflammation and Pain Following Cataract Surgery

NCT01591655

COMPLETED NA

Evaluation of Ocular Comfort With ISTA Tears vs Systane

NCT01650584

COMPLETED NA

A Study to Evaluate the Product Feasibility of Two New Silicone Hydrogel Contact Lenses

NCT01583868

COMPLETED Phase 3

Therapeutic Equivalence Study of Generic Brinzolamide vs Azopt

NCT01722604

COMPLETED NA

A Study to Evaluate the Feasibility of a High Add Multi Focal Contact Lens

NCT01518868

COMPLETED NA

A Study to Evaluate the Product Performance of a Low Add MultiFocal Soft Contact Lens

NCT01539694

COMPLETED Phase 2

Bepotastine Besilate-corticosteroid Nasal Spray Combination Compared to Placebo, Bepotastine Besilate Nasal Spray, and Corticosteroid Nasal Spray in the Treatment of Patients With Seasonal Allergic Rhinitis

NCT01578278

COMPLETED NA

A Study to Evaluate the Product Feasibility of a New Silicone Hydrogel Contact Lens

NCT01412983

COMPLETED NA

A Study to Evaluate the Product Performance of the PureVision®2 High Definition (HD) Contact Lens

NCT01416142

COMPLETED NA

Safety and Efficacy of a Contact Lens for Daily Disposable Use

NCT01365039

COMPLETED Phase 3

Efficacy of Bromfenac Ophthalmic Solution in Patients Undergoing Cataract Surgery

NCT01367249

TERMINATED Phase 3

Besifloxacin Ophthalmic Suspension Verses Gatifloxacin Ophthalmic Solution in Neonates With Bacterial Conjunctivitis

NCT01330355

COMPLETED NA

A Study to Evaluate a Modified Contact Lens

NCT01391364

TERMINATED NA

Twelve Month Clinical Evaluation of KeraSoft IC Soft Contact Lenses

NCT01416272

COMPLETED Phase 2

Mapracorat Ophthalmic Formulation in Subjects With Allergic Conjunctivitis

NCT01289431

TERMINATED

Tear Evaluation Between Habitual Contact Lens Wearers and Non Contact Lens Wearers

NCT01317030

TERMINATED Phase 3

Mapracorat Ophthalmic Suspension, 3% for the Treatment of Ocular Inflammation Following Cataract Surgery

NCT01298752

COMPLETED NA

Evaluation of Two Daily Disposable Contact Lenses.

NCT01300065

COMPLETED Phase 2

Study Comparing the Safety and Efficacy of BOL-303259-X to Latanoprost in Subjects With Glaucoma or Ocular Hypertension

NCT01223378

COMPLETED NA

A Study to Evaluate a New Silicone Hydrogel Contact Lens

NCT01309893

COMPLETED NA

Evaluation of a New Silicone Hydrogel Contact Lens

NCT01309880

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Phase Distribution

PhaseTrial count
Phase 1 16
Phase 2 26
Phase 3 46
Phase 4 14

What the Pipeline for Bausch & Lomb Incorporated Shows

According to the ClinicalTrials.gov registry, Bausch & Lomb Incorporated is linked to 174 US clinical trials across every stage of research activity. Of those, 3 studies are currently recruiting, about 2% of the sponsor's indexed portfolio, and 158 are already marked complete, representing roughly 91% of the total.

The phase mix for Bausch & Lomb Incorporated reports 60 late-stage studies (Phase 3 and Phase 4 combined) and 42 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Bausch & Lomb Incorporated is Myopia with 9 linked trials, and 9 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.