Bausch & Lomb Incorporated
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
Corneal Endothelial Cell Density Changes In Healthy Subjects, When Administered ISV-403 for 5 Days
NCT01120418
Dose-Finding Study Comparing the Safety and Efficacy of Latanoprost to a Novel Treatment for Glaucoma
NCT00441883
Evaluation of the Onset and Duration of Action of Bepotastine Besilate Ophthalmic Solution in Acute Allergic Conjunctivitis
NCT00424398
Zylet vs TobraDex in Blepharokeratoconjunctivitis
NCT00447577
Pediatric Zylet Safety and Efficacy Study
NCT00420628
Efficacy and Safety of Topical Bromfenac Ophthalmic Solution vs. Placebo in Subjects With Allergic Conjunctivitis
NCT00423007
Systemic Pharmacokinetics of BOL-303224-A
NCT00407589
Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome
NCT00370747
A Study to Evaluate Plasmin for the Creation of a Posterior Vitreous Detachment (PVD)
NCT00347646
Safety/Efficacy of Bromfenac Ophthalmic Solution for Ocular Inflammation and Pain Associated With Cataract Surgery
NCT00333918
Study to Evaluate Plasmin for the Creation of a Posterior Vitreous Detachment
NCT00348439
Loteprednol Etabonate Opthalmic Suspension for the Treatment of Dry Eye
NCT00560638
A Clinical Evaluation of the Next Generation Diagnostic Instrument (NGDI)
NCT00347594
Assessment of Intravitreous Injections of Vitrase for Inducing Posterior Vitreous Detachment
NCT00198471
A Bioequivalence Study of Tobramycin and Prednisolone Acetate Compared to PredForte
NCT00198523
A Study to Evaluate the Safety and Effectiveness of the Technols 217z Zyoptix System for Hyperopia
NCT00348205
Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome
NCT00198536
Evaluation of Vitrase as a Spreading Agent
NCT00198484
Evaluation of Vitrase as an Adjuvant to Increase Absorption and Dispersion of Other Injected Anesthetics
NCT00198549
Hypersensitivity Reaction to Vitrase (Ovine Hyaluronidase)
NCT00198458
Hypersensitivity Reaction to Vitrase (Ovine Hyaluronidase)
NCT00198419
Safety and Efficacy Study of Topical Bromfenac Versus Placebo to Treat Ocular Inflammation After Cataract Surgery
NCT00198445
Safety and Efficacy of Fluocinolone Acetonide Intravitreal Implants
NCT00407082
Safety and Efficacy Study of Vitrase for Clearance of Severe Vitreous Hemorrhage
NCT00198510
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 16 |
| Phase 2 | 26 |
| Phase 3 | 46 |
| Phase 4 | 14 |
Therapeutic Areas
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.
Read our methodology - how this data is sourced, computed, and verified.
Related
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.