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 3 of 4

COMPLETED NA

A Study to Evaluate the Performance of Two Designs of Soft Toric Lenses

NCT01309867

COMPLETED Phase 2

Safety and Efficacy of Bepotastine Besilate Nasal Spray in the Treatment of Seasonal Allergic Rhinitis

NCT01277341

COMPLETED NA

Evaluation of the Feasibility a New Silicone Hydrogel Contact Lens

NCT01309906

COMPLETED Phase 3

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

NCT01230125

COMPLETED NA

Product Feasibility of a New Silicone Hydrogel Contact Lens

NCT01309100

COMPLETED NA

Study of A New Contact Lens Cleaning and Disinfecting Solution

NCT01318577

COMPLETED Phase 3

One-Piece Hydrophobic Acrylic Intraocular Lens in Subjects Undergoing Cataract Extraction

NCT01230060

COMPLETED NA

Study to Evaluate a Contact Lens Lubricating and Rewetting Drop

NCT01267656

TERMINATED Phase 4

Accommodation Measurements After Bilateral Implantation of an Aspheric Accommodating Lens and Monofocal Aspheric Lenses

NCT01241279

COMPLETED Phase 3

A Dose Ranging Study to Evaluate Safety and Efficacy of Bromfenac Ophthalmic Solution in Dry Eye Disease

NCT01212471

COMPLETED NA

A Study to Evaluate the Product Performance of a Daily Disposable Contact Lens

NCT01192126

COMPLETED Phase 2

Study to Assess the Safety and Efficacy of BOL-303242-X Ophthalmic Suspension in Dry Eye Syndrome

NCT01163643

COMPLETED NA

Toric Intraocular Lens Following Cataract Surgery

NCT01140477

COMPLETED Phase 4

Evaluation of 3 Intraocular Lenses Following Lens Extraction

NCT01122576

COMPLETED Phase 3

Safety of Besivance™ (Besifloxacin Ophthalmic Suspension) 0.6% Compared to Vehicle

NCT01175590

COMPLETED Phase 2

Safety and Efficacy of Bepotastine Besilate Ophthalmic Solution in Seasonal Allergic Conjunctivitis Patients

NCT01174823

COMPLETED NA

Evaluation of Two Different Designs of Bausch & Lomb Contact Lenses

NCT01118338

COMPLETED Phase 1

Safety, Pharmacokinetics, and Efficacy of Bepotastine Besilate Nasal Product After Ragweed Pollen Exposure in an Environmental Chamber

NCT01222299

COMPLETED NA

Feasibility of a New Silicone Hydrogel Lens

NCT01131130

COMPLETED Phase 4

Extension Study to Gather Data on Effect of Macugen on the Corneal Endothelium

NCT01573572

COMPLETED Phase 2

Loteprednol Ophthalmic Base Compared to Loteprednol Ophthalmic Suspension vs Placebo in an Allergen Challenge

NCT01107405

COMPLETED NA

A Study to Assess the Safety and Efficacy of a Daily Disposable Contact Lens

NCT01130974

COMPLETED Phase 3

Evaluation of Loteprednol Etabonate Versus Vehicle for the Treatment of Inflammation and Pain Following Cataract Surgery

NCT01060072

COMPLETED Phase 3

Ketotifen/Naphazoline Ophthalmic Solution in the Conjunctival Allergen Challenge Model of Acute Allergic Conjunctivitis.

NCT00770133

COMPLETED Phase 3

Loteprednol Etabonate Versus Vehicle for the Treatment of Inflammation and Pain Following Cataract Surgery

NCT01010633

COMPLETED NA

A Study to Evaluate the Clinical Performance of a Novel Multipurpose Solution

NCT01024751

COMPLETED Phase 2

Efficacy of Besifloxacin Ophthalmic Suspension in the Treatment of Bacterial Conjunctivitis

NCT00972777

COMPLETED NA

Performance Evaluation of Contact Lenses Among a Population of Adapted Contact Lens Wearers

NCT00985231

COMPLETED Phase 2

Evaluation of BOL-303242-X Versus Vehicle for the Treatment of Inflammation Following Cataract Surgery

NCT00905450

COMPLETED Phase 1

Concentration of Besifloxacin, Gatifloxacin, and Moxifloxacin in Human Conjunctiva After Topical Instillation

NCT00905762

COMPLETED Phase 3

Study of T-PRED(TM) Compared to Pred Forte(R) II

NCT00854061

COMPLETED Phase 1

Assessment of the Concentrations of Besifloxacin, Moxifloxacin, or Gatifloxacin in the Aqueous Humor of Subjects

NCT00824070

COMPLETED Phase 3

Efficacy Study of Bromfenac Ophthalmic Solution in Patients Undergoing Cataract Surgery

NCT00853970

COMPLETED NA

A Product Performance Evaluation of a Novel Contact Lens for Daily Disposable Use

NCT00784641

COMPLETED NA

One-Day Dispensing Clinical Evaluation of SofLens Daily Disposable Lenses Compared to a Marketed 1 Day Contact Lens

NCT00902850

COMPLETED Phase 3

Ketotifen/Naphazoline Ophthalmic Solution in the Conjunctival Allergen Challenge Model of Allergic Conjunctivitis.

NCT00769886

COMPLETED Phase 2

Safety and Efficacy of an Ophthalmic Solution in Dry Eye Disease

NCT00758784

COMPLETED NA

Evaluation of a Multi-Purpose Solution

NCT00710879

COMPLETED Phase 3

Loteprednol Etabonate in an Ophthalmic Base vs Vehicle for the Treatment of Inflammation Following Cataract Surgery

NCT00699153

COMPLETED Phase 3

Efficacy and Safety of Bromfenac Ophthalmic Solution in Cataract Surgery

NCT00704418

COMPLETED Phase 3

Efficacy and Safety of Bromfenac Ophthalmic Solution in Cataract Surgery

NCT00703781

COMPLETED Phase 4

Safety and Efficacy of Zylet vs Lotemax, Tobramycin and Vehicle in Pediatric Blepharoconjunctivitis

NCT00705159

COMPLETED Phase 2

Study of T-PRED(TM) Compared to Pred Forte(R)

NCT00699803

COMPLETED Phase 2

Efficacy Study of Ecabet Ophthalmic Solution in Dry Eye Disease

NCT00667004

COMPLETED NA

Safety and Efficacy of a Bausch & Lomb Multipurpose Solution When Compared to Ciba Vision Aquify Multipurpose Solution

NCT00636363

COMPLETED Phase 3

Loteprednol Etabonate Ophthalmic Ointment vs. Vehicle in the Treatment of Inflammation Following Cataract Surgery

NCT00645671

COMPLETED NA

Performance of Bausch & Lomb ReNu MultiPlus Multi-Purpose Solution in a New Packaging Configuration

NCT00659815

COMPLETED Phase 4

Comparative Performance of PureVision, Acuvue Oasys and O2Optix

NCT00640341

COMPLETED Phase 2

Efficacy and Safety of Bromfenac Ophthalmic Solution

NCT00585975

COMPLETED Phase 3

Efficacy and Safety Study of Bepotastine Besilate Ophthalmic Solution in Allergic Conjunctivitis

NCT00586664

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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.