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 1 of 4

RECRUITING Phase 2

Phase 2 Study of BL1107 Eye Drops vs. Timolol in Adults With Primary Open Angle Glaucoma or Ocular Hypertension

NCT07168902

RECRUITING Phase 2

A Study Evaluating the Safety and Efficacy of a Fixed-Dose Combination for Dry Eye Disease

NCT07128628

RECRUITING

IC-8 Apthera IOL New Enrollment Post Approval Study

NCT06060041

ACTIVE NOT RECRUITING Phase 1

A Study to Assess Safety, Tolerability, and Pharmacokinetics of Ascending Concentrations of Topical Ocular BL1332 in Healthy Volunteers

NCT06978244

ACTIVE NOT RECRUITING NA

Study to Evaluate the Safety and Effectiveness of the enVista® Beyond (EY) EDF Intraocular Lens in Subjects Undergoing Cataract Extraction

NCT06333015

ACTIVE NOT RECRUITING Phase 4

A Study to Evaluate Corneal Endothelial Cell Density (ECD) in Subjects With Dry Eye Disease (DED) Administering Miebo® (Perfluorohexyloctane Ophthalmic Solution) for 12 Months.

NCT06565650

ACTIVE NOT RECRUITING NA

Safety and Effectiveness of the TENEO 317 Model 2 (1.28 US) Excimer Laser for Laser In Situ Keratomileusis (LASIK) Surgery to Treat Hyperopia With or Without Astigmatism

NCT05264623

NOT YET RECRUITING

Revive Toric RWE Study

NCT06785194

COMPLETED Phase 4

A Study to Evaluate Concomitant Perfluorohexyloctane Use With Contact Lens Wear

NCT07054606

COMPLETED Phase 3

A Study Comparing the Efficacy and Safety of Brimonidine Tartrate Ophthalmic Solution 0.025% With Sodium Hyaluronate Relative to Lumify in Adult Subjects With Ocular Redness

NCT06803654

COMPLETED NA

A Study to Evaluate Real World Outcomes of the enVista® Aspire (EA) and Aspire Toric (ETA) Intraocular Lens in Subjects Undergoing Cataract Extraction

NCT06594185

COMPLETED

A Study to Evaluate the enVista® Aspire (EA) Intraocular Lens in Subjects Undergoing Cataract Extraction

NCT06333028

COMPLETED Phase 4

A Study to Evaluate the Effect of Miebo™ on Preoperative Biometry/Keratometry and Postoperative Refractive Accuracy

NCT06346340

COMPLETED Phase 4

A Study to Evaluate Early Treatment Outcomes With Miebo™ in Subjects With Dry Eye Disease

NCT06309953

COMPLETED NA

1-Week Dispensing Evaluation of REVIVE™ Toric Soft Contact Lenses

NCT06053736

COMPLETED NA

Kalifilcon A Toric Compared to Commercially Available Lenses

NCT06098937

COMPLETED Phase 4

Effects of NOV03 on the Tear Film

NCT05723770

COMPLETED NA

Orientation Characteristics of Daily Disposable Toric Contact Lenses

NCT06069609

COMPLETED NA

Study of Safety and Effectiveness of the Boston Orthokeratology Shaping Lens in the Arise Orthokeratology Lens

NCT05984290

COMPLETED Phase 3

Evaluation of the Safety and Pharmacokinetics of Brimonidine Tartrate 0.025%/Ketotifen Fumarate 0.035% Combination Ophthalmic Solution

NCT05815758

COMPLETED NA

A Study to Evaluate the Safety and Effectiveness of a Contact Lens Cleaning and Disinfecting Solution

NCT05565937

COMPLETED Phase 3

Evaluation of Brimonidine Tartrate/Ketotifen Fumarate Combination in Adults With Seasonal Allergic Conjunctivitis

NCT05591755

COMPLETED NA

Evaluation of Product Performance of a New Silicone Hydrogel Multifocal Contact Lens

NCT05660577

COMPLETED Phase 3

Evaluation of Brimonidine Tartrate/Ketotifen Fumarate Combination for the Treatment of Allergic Conjunctivitis

NCT05579730

COMPLETED Phase 3

"Efficacy and Safety of Brimonidine Tartrate Preservative-Free Formulation in Adults With Ocular Redness"

NCT05360784

COMPLETED NA

1-Week Dispensing Evaluation of Kalifilcon A Daily Disposable Multifocal Compared to Ultra for Presbyopia

NCT05325931

COMPLETED NA

1-Week Dispensing Evaluation of Kalifilcon A Toric Contact Lenses Compared to Ultra for Astigmatism

NCT05320042

COMPLETED NA

Insertion Clinical Study to Evaluate the Orientation Characteristics of Multiple Kalifilcon A Daily Disposable Toric LD213001 Contact Lenses

NCT05129124

COMPLETED NA

2-Hour Dispensing Evaluation of Samfilcon A Lenses With EPG01 Packaging Solution Compared to Commercially Available B+L Ultra Lenses

NCT05126953

COMPLETED NA

Biotrue ONEday Contact Lenses With EPG03 Packaging Solution Compared to Biotrue ONEday Contact Lenses

NCT05129488

COMPLETED NA

Insertion Clinical Study to Evaluate the Aberration Characteristics of Kalifilcon A Toric Lenses

NCT05129072

COMPLETED NA

Surface Refractive Index Shift and Lens Absorption/Adsorption of Tear Components of Kalifilcon A Lenses vs Dailies Total1 and Precision1

NCT04840563

COMPLETED Phase 3

Effect of NOV03 on Signs and Symptoms of Dry Eye Disease Associated With Meibomian Gland Dysfunction (Mojave Study)

NCT04567329

COMPLETED Phase 3

Long-Term Safety and Tolerability of NOV03 (Perfluorohexyloctane) in Subjects Who Completed Trial NVU-003 (Kalahari Study)

NCT04140227

COMPLETED NA

Evaluation of Surface Refractive Index Shift of Kalifilcon A Lenses Compared to Dailies Total 1, Precision 1 and Biotrue ONEday Lenses

NCT04555031

COMPLETED

Evaluation of Visual Acuity of the Envista One-piece Acrylic Toric IOL MX60ET

NCT05739656

COMPLETED Phase 3

Perfluorohexylcotane (NOV03) for the Treatment of Signs and Symptoms of Dry Eye Disease Associated With Meibomian Gland Dysfunction (Gobi Study)

NCT04139798

COMPLETED NA

A Study of B + L Ophthalmic Viscosurgical Device (OVD) CVisc50

NCT04192630

COMPLETED Phase 1

Safety and IOP-Lowering Effects of WB007

NCT04149899

COMPLETED NA

A Safety and Effectiveness Study of a New Preservative Free Rewetting Drop

NCT04175340

COMPLETED NA

Product Performance of a New Silicone Hydrogel Contact Lens

NCT04901897

COMPLETED NA

A Study With Technolas® TENEO 317 Model 2 Excimer Laser to Treat Participants With Myopia or Myopic Astigmatism

NCT04111757

COMPLETED NA

A Study to Evaluate the Safety and Efficacy of Kalifilcon A Daily Disposable Contact Lens

NCT04158466

COMPLETED NA

A Safety and Effectiveness Study of BL-ABT12 Multi-Purpose Solution for Use by Participants With Soft Contact Lenses

NCT03897751

COMPLETED NA

A Study to Evaluate the Safety and Effectiveness of a Silicone Hydrogel Custom Contact Lens When Compared to Alden Optical HP Sphere Lens

NCT03897712

COMPLETED NA

Evaluate the Safety and Effectiveness of the Biotrue ONEday for Astigmatism

NCT03681808

COMPLETED NA

Evaluate the Safety and Effectiveness of the enVista® One-Piece Hydrophobic Acrylic Trifocal Intraocular Lens

NCT03603600

COMPLETED NA

Bausch & Lomb Ophthalmic Viscosurgical Device (OVD) Dispersive (DVisc40)

NCT03511638

COMPLETED Phase 3

A Single-Center Evaluation of the Relative Efficacy of EM-100 Compared to Zaditor® (Ketotifen Fumarate Ophthalmic Solution 0.035%) and Vehicle

NCT03489941

COMPLETED Phase 1

Therapeutic Equivalence Study of Generic Brinzolamide vs Azopt

NCT03896633

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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.