Bausch & Lomb Incorporated

Open enrollment across a mixed-phase pipeline

According to ClinicalTrials.gov-derived indexes, Bausch & Lomb Incorporated sits in the top decile of US sponsors by registered trial count (#170 of 15,742 sponsors by registered trial count).

174 total trials 3 currently recruiting 158 completed top decile by trial count

Bausch & Lomb Incorporated: 174 sponsored US clinical trials, 3 recruiting.

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.

Top-decile sponsor footprint

Bausch & Lomb Incorporated ranks in the top decile of sponsors by registered trial count (#170 of 15,742 sponsors by registered trial count). Volume at this scale usually reflects a long institutional pipeline, read phase tilt and therapeutic areas below before treating it as current-year activity.

Trial completion reliability score

C 78/100

158 of 166 decided trials (Completed vs. Terminated on ClinicalTrials.gov) reached their planned completion (95.2%), vs. national p10 68.4% / p90 100% among 1,234 sponsors with at least 10 decided trials. Still-open trials (Recruiting, Active-not-recruiting, Not-yet-recruiting) are excluded since they have not reached an outcome yet.

Open and recent trials

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 is open in the Bausch & Lomb Incorporated pipeline

3 recruiting of 174 indexed (2% open); 158 completed (91%).

Phase mix: 60 late (III/IV) vs 42 early (I/II) (balanced across stages).

Top condition: Myopia (9 trials), 9 others listed.

How open-pipeline share is computed

Recruiting share is recruiting_count divided by trial_count for this sponsor in the public registry export. Status can change between pulls; treat the figure as a research-attention snapshot, not product availability.

Bausch & Lomb Incorporated: open-pipeline peers nationwide

Peers matched on 174 registered trials and 2% open enrollment, not the therapeutic-area sidebar.

Bausch & Lomb Incorporated sits below the median trial volume and below the median recruiting share among these 9 nationwide peers -- the two do not always move together. Source: ClinicalTrials.gov (2026-08-08 snapshot). 2×2 strategic matrix plotting 9 entities by Total trials (X) and Recruiting share (Y), with a crosshair dividing the plot into four quadrants. Higher volume & more openFocused & more openHigher volume, mostly closedSmaller & mostly closed 0100200300 0%5%10%15%20% Total trials Recruiting share Bausch & Lomb IncorporatedAlbert Einstein College of MedicineUConn HealthTufts Medical CenterBaylor Research InstituteMedtronic Cardiac Rhythm and Heart FailureEisaiLexicon PharmaceuticalsAlcon Research
Bausch & Lomb Incorporated sits below the median trial volume and below the median recruiting share among these 9 nationwide peers -- the two do not always move together. Source: ClinicalTrials.gov (2026-08-08 snapshot).

Bausch & Lomb Incorporated sits below the median trial volume and below the median recruiting share among these 9 nationwide peers -- the two do not always move together.

Sponsors near 174 trials (± recruiting share)

Sponsors near 2% open enrollment (± trial volume)

What to do with this Bausch & Lomb Incorporated page

174 registered trials is a research-attention snapshot, not an endorsement of Bausch & Lomb Incorporated or any single study.

  • 3 of Bausch & Lomb Incorporated's trials are currently recruiting, check each one's own eligibility criteria before contacting a site. Browse recruiting trials
  • Myopia is the condition Bausch & Lomb Incorporated studies most, compare against other sponsors active in the same condition before evaluating a specific study. See Myopia trials
  • Bring the specific trial ID (NCT number) to your own doctor before enrolling, this page is a directory, not medical guidance. Read the trial-finding guide

Trial and recruiting counts reflect ClinicalTrials.gov registry status as of the data vintage above; individual trial eligibility and enrollment status can change.

Bausch & Lomb Incorporated pipeline card: 174 registered trials from official public datasets.Report a data error.