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 4 of 4

COMPLETED Phase 1

Corneal Endothelial Cell Density Changes In Healthy Subjects, When Administered ISV-403 for 5 Days

NCT01120418

COMPLETED Phase 2

Dose-Finding Study Comparing the Safety and Efficacy of Latanoprost to a Novel Treatment for Glaucoma

NCT00441883

COMPLETED Phase 2

Evaluation of the Onset and Duration of Action of Bepotastine Besilate Ophthalmic Solution in Acute Allergic Conjunctivitis

NCT00424398

COMPLETED Phase 4

Zylet vs TobraDex in Blepharokeratoconjunctivitis

NCT00447577

COMPLETED Phase 4

Pediatric Zylet Safety and Efficacy Study

NCT00420628

COMPLETED Phase 3

Efficacy and Safety of Topical Bromfenac Ophthalmic Solution vs. Placebo in Subjects With Allergic Conjunctivitis

NCT00423007

COMPLETED Phase 1

Systemic Pharmacokinetics of BOL-303224-A

NCT00407589

COMPLETED Phase 2

Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome

NCT00370747

TERMINATED Phase 1

A Study to Evaluate Plasmin for the Creation of a Posterior Vitreous Detachment (PVD)

NCT00347646

COMPLETED Phase 3

Safety/Efficacy of Bromfenac Ophthalmic Solution for Ocular Inflammation and Pain Associated With Cataract Surgery

NCT00333918

TERMINATED Phase 2

Study to Evaluate Plasmin for the Creation of a Posterior Vitreous Detachment

NCT00348439

COMPLETED Phase 2

Loteprednol Etabonate Opthalmic Suspension for the Treatment of Dry Eye

NCT00560638

COMPLETED NA

A Clinical Evaluation of the Next Generation Diagnostic Instrument (NGDI)

NCT00347594

COMPLETED Phase 2

Assessment of Intravitreous Injections of Vitrase for Inducing Posterior Vitreous Detachment

NCT00198471

COMPLETED Phase 3

A Bioequivalence Study of Tobramycin and Prednisolone Acetate Compared to PredForte

NCT00198523

COMPLETED NA

A Study to Evaluate the Safety and Effectiveness of the Technols 217z Zyoptix System for Hyperopia

NCT00348205

COMPLETED Phase 2

Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome

NCT00198536

COMPLETED Phase 3

Evaluation of Vitrase as a Spreading Agent

NCT00198484

COMPLETED Phase 4

Evaluation of Vitrase as an Adjuvant to Increase Absorption and Dispersion of Other Injected Anesthetics

NCT00198549

COMPLETED Phase 1

Hypersensitivity Reaction to Vitrase (Ovine Hyaluronidase)

NCT00198458

COMPLETED Phase 1

Hypersensitivity Reaction to Vitrase (Ovine Hyaluronidase)

NCT00198419

COMPLETED Phase 3

Safety and Efficacy Study of Topical Bromfenac Versus Placebo to Treat Ocular Inflammation After Cataract Surgery

NCT00198445

COMPLETED Phase 2

Safety and Efficacy of Fluocinolone Acetonide Intravitreal Implants

NCT00407082

COMPLETED Phase 3

Safety and Efficacy Study of Vitrase for Clearance of Severe Vitreous Hemorrhage

NCT00198510

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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.