Alcon Research

111 total trials 32 currently recruiting 77 completed

Trial Pipeline

RECRUITING NA

Feasibility Study of an Accommodating IOL Design

NCT07147192

RECRUITING NA

Post Market Clinical Evaluation of Clareon PanOptix Pro and Clareon PanOptix Pro Toric IOLs

NCT07161635

RECRUITING Phase 1

Study of AR-14034 in Participants With Neovascular Age-Related Macular Degeneration (nAMD)

NCT05769153

RECRUITING NA

Hydrus® Microstent New Enrollment Post-Approval Study

NCT04553523

ACTIVE NOT RECRUITING Phase 3

Reformulated PG324 Ophthalmic Solution for Intraocular Pressure Reduction

NCT07082816

ACTIVE NOT RECRUITING NA

Post Market Clinical Follow-up (PMCF) Study of Clareon Vivity & Clareon PanOptix

NCT05796453

COMPLETED Phase 3

A Study Designed to Evaluate Tear Production

NCT06544707

COMPLETED Phase 3

A Study to Investigate the Effect of 0.003% AR-15512 on Subjects With Dry Eye Disease

NCT06544694

COMPLETED NA

Clareon PanOptix Pro vs. Clareon PanOptix - Study B

NCT06401551

COMPLETED

Air Optix Daily Wear Contact Lenses

NCT05827224

COMPLETED NA

Assessing the Clinical Performance of Two Frequent Replacement Silicone Hydrogel Multifocal Toric Contact Lenses

NCT05886907

COMPLETED NA

The Clinical Performance of Two Reusable Silicone Hydrogel Contact Lenses

NCT05766787

COMPLETED

Air Optix Night and Day Aqua (AONDA) Retrospective Study 1

NCT05790928

COMPLETED NA

Clinical Evaluation of a Manufacturing Process for a Frequent Replacement Silicone Hydrogel Multifocal Contact Lens

NCT05765227

COMPLETED NA

Clareon Toric vs Eyhance Toric

NCT05481125

COMPLETED NA

Clinical Performance Evaluation of Two Frequent Replacement Silicone Hydrogel Multifocal Contact Lenses

NCT05338333

COMPLETED NA

Clinical Performance of Two Commercial, Daily Disposable Contact Lenses

NCT05010512

COMPLETED NA

Clinical Investigation of the WaveLight® EX500 Excimer Laser

NCT04805593

COMPLETED NA

Three Daily Wear Monthly Replacement Silicone Hydrogel Contact Lenses With Two Multi-purpose Disinfecting Solution Combinations

NCT04789382

COMPLETED NA

Clinical Characterization of an Investigational Frequent Replacement Daily Wear Silicone Hydrogel Sphere Contact Lens

NCT04702984

COMPLETED NA

Clinical Assessment of a Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lens

NCT04476784

COMPLETED NA

Assessment of an Investigational Frequent Replacement Silicone Hydrogel Lens

NCT04085328

COMPLETED NA

Comparison of Two Daily Disposable Lenses

NCT04013789

COMPLETED NA

Comparison Between iLux and LipiFlow in the Treatment of Meibomian Gland Dysfunction (MGD): A 12-month, Multicenter Study

NCT03956225

COMPLETED NA

Clinical Performance of a Monthly Replacement Silicone Hydrogel Lens

NCT03586167

COMPLETED NA

Clinical Performance of a Silicone Hydrogel Contact Lens Following One Night of Extended Wear

NCT03560141

COMPLETED NA

Clinical Investigation of AcrySof® IQ PanOptix™ IOL Model TFNT00

NCT03280108

COMPLETED NA

DD T2 Daily Disposable Registration Trial

NCT03305770

COMPLETED NA

A Clinical Study of the ACRYSOF® IQ Extended Depth of Focus Intraocular Lens (IOL)

NCT03274986

COMPLETED NA

Clinical Investigation of the Clareon® Intraocular Lens (IOL)

NCT03170154

COMPLETED NA

Assessing Fitting Guides in Alcon Multifocal Contact Lenses

NCT03118934

COMPLETED NA

Early Feasibility Study of UV-Femtosecond Laser Assisted Lenticular Extraction

NCT03021707

COMPLETED NA

Comparative In-Vivo Wetting Characteristics of Silicone Hydrogel Materials With Selected Lens Care Systems

NCT01699750

COMPLETED Phase 2

Evaluation of AL-78898A in Exudative Age-Related Macular Degeneration

NCT01157065

COMPLETED NA

Lens Wearing Experience and Biocompatibility of a Multi-Purpose Disinfecting Solution (MPDS)

NCT01476722

COMPLETED Phase 2

ESBA105 in Patients With Severe Dry Eye

NCT01338610

COMPLETED Phase 4

AZARGA Transition Study in Taiwan for Patients With Uncontrolled Intraocular Pressure

NCT01484951

COMPLETED NA

Evaluation of Extended Tear Film Break Up Time (TFBUT) With an Ocular Emulsion

NCT01368198

COMPLETED Phase 4

Assessment of Alcon's Ocular Image Quantification System

NCT01282138

COMPLETED NA

Effect of FID 114675A on Lens Wettability

NCT01342107

COMPLETED NA

Alcon Multi-Purpose Disinfecting Solution Versus Renu Fresh Multi-Purpose Solution in Symptomatic Contact Lens Wearers

NCT01187355

COMPLETED Phase 4

A Comparison of Visual Function After Bilateral Implantation of Presbyopia-correcting Intraocular Lenses (IOLs)

NCT01166971

COMPLETED Phase 2

Travoprost Five Day Posology Study

NCT01114893

COMPLETED Phase 3

A Study to Evaluate the Clinical Efficacy and Safety of Tobradex® ST Compared to Azasite® in the Treatment of Subjects With Moderate to Severe Chronic Blepharitis

NCT01102244

COMPLETED Phase 4

Assessing the Efficacy of Maxidex® and Patanol® for the Treatment of Allergic Conjunctivitis

NCT01119287

COMPLETED NA

Assessment of Tear Film-Based Proteins Associated With Care Solution Induced Corneal Staining

NCT01100424

COMPLETED NA

A Comparison of Corneal Aberrations in Subjects With Contralateral AcrySof IQ Toric Intraocular Lens (IOL) and AcrySof IQ IOL With Limbal Relaxing Incision (LRI)

NCT01045733

COMPLETED NA

Safety and Efficacy of an Investigational Multi-Purpose Disinfecting Solution

NCT01341977

COMPLETED NA

ACRYSOF® Toric NATURAL T9 Intraocular Lens (IOL)

NCT00967473

COMPLETED Phase 4

Comparison of Seasonal Allergic Rhinitis Treatment With 2 Antihistamines Used in Combination With Intranasal Corticosteroid

NCT00845195

COMPLETED

Corneal Astigmatism Measurement Study

NCT00818532

COMPLETED Phase 4

Evaluation of the Sensory Attributes of Olopatadine 0.6% and Azelastine 137mcg Nasal Sprays in Patients w/Allergic Rhinitis

NCT00772304

COMPLETED Phase 4

Study of the Progression of Bacterial Conjunctivitis Symptoms Upon Antibiotic Treatment

NCT00798577

COMPLETED NA

A Multi-Center Investigation of Patient Acceptability of OPTI-FREE RepleniSH® Multi-Purpose Disinfecting Solution (MPDS)

NCT00772707

COMPLETED Phase 4

Study of Efficacy and Safety of Vigadexa in Treating Inflammation and Infection Post-cataract Surgery

NCT00870103

COMPLETED

Defining the Conjunctival Staining Method: Instillation Volume and Time Course to Assess Staining With Lissamine Green

NCT00768898

COMPLETED Phase 2

Anecortave Acetate Safety in Patients With Open-Angle Glaucoma or Ocular Hypertension

NCT00691717

COMPLETED NA

Evaluation of SYSTANE Ultra Lubricant Eye Drops

NCT00702377

COMPLETED NA

Acute Comfort of Lubricant Eye Drops FID 112903

NCT00673855

COMPLETED NA

Rotational Stability of the AcrySof® Toric

NCT00762216

COMPLETED Phase 4

Comparison of Olopatadine 0.6% and Fluticasone Proprionate 50mcg Nasal Sprays in a Two Week Seasonal Allergic Rhinitis Trial

NCT00691665

COMPLETED Phase 4

To Compare the Ability of DiscoVisc® OVD to Protect the Corneal Endothelium and Maintain Anterior Chamber Space With Healon® and Amvisc® PLUS During Cataract Surgery.

NCT00763360

COMPLETED Phase 3

Safety and Efficacy of Olopatadine HCl Nasal Spray in 6-11 Year Old Patients

NCT00578929

COMPLETED

Surgeon Experience ReSTOR A +4 Intraocular Lens (IOL)

NCT00733512

COMPLETED Phase 4

Examining The Efficacy, Safety And Improved Tolerability Of Travoprost BAK Free Ophthalmic Solution (Travatan-Z) Compared To Prior Prostaglandin Therapy

NCT00444665

COMPLETED NA

Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL

NCT00759096

COMPLETED NA

Visual Function and Patient Satisfaction After Bilateral Implantation of AcrySof Natural ReSTOR (Model SN60D3) or AcrySof Natural Monofocal (Model SN60AT)

NCT00759668

COMPLETED Phase 3

DisCoVisc Comparative Evaluation

NCT00732225

COMPLETED Phase 4

Visual Function After Bilateral Implantation of AcrySof® Toric

NCT00758550

COMPLETED Phase 3

A Phase IIIb Study of DuoTrav to Treat Glaucoma or Ocular Hypertension

NCT00465803

COMPLETED NA

Posterior Capsule Opacification (PCO) Evaluation of the AcrySof SN60AT Lens vs. SN60WF Lens

NCT00762021

COMPLETED Phase 3

Safety Study of Olopatadine Nasal Spray

NCT00578331

COMPLETED Phase 3

AL-15469A for the Treatment of Bacterial Conjunctivitis

NCT00332293

COMPLETED Phase 4

A Comparison of Topical Nepafenac to Placebo in Corneal Epithelial Healing Times and Postoperative Pain Relief

NCT00330798

COMPLETED Phase 2

Anecortave Acetate for Treatment of Steroid Induced Intraocular Pressure (IOP) Elevation

NCT00315640

COMPLETED Phase 3

AL-15469A for the Treatment of Bacterial Conjunctivitis

NCT00331916

COMPLETED Phase 3

Anecortave Acetate in Patients With Exudative Age-related Macular Degeneration (AMD)

NCT00299507

COMPLETED NA

Effect of Multi-Purpose Solutions on Ex-Vivo Wetting Angles

NCT00383201

COMPLETED NA

Evaluation of an Investigational Multi-Purpose Disinfecting Solution for the Care of Soft Contact Lenses in Symptomatic Patients

NCT00382603

COMPLETED NA

Evaluation of an Investigational Multi-Purpose Disinfecting Solution for the Care of Silicone Hydrogel Soft Contact Lenses

NCT00382902

COMPLETED Phase 3

An Evaluation of Safety and Efficacy of Anecortave Acetate Versus Placebo in Patients With Subfoveal CNV Due to Exudative AMD

NCT00058994

COMPLETED Phase 3

Phase 3 Study to Evaluate IOP Lowering Therapy in Open Angle Glaucoma and Ocular Hypertension C-01-70

NCT00047541

COMPLETED Phase 3

A 6-Week Safety and Efficacy Study of Travatan Compared to Xalcom in Subjects With Open-Angle Glaucoma(OAG) or Ocular Hypertension(OHT)

NCT00051155

Phase Distribution

PhaseTrial count
Phase 1 29
Phase 2 5
Phase 3 14
Phase 4 13

What the Pipeline for Alcon Research Shows

According to the ClinicalTrials.gov registry, Alcon Research is linked to 111 US clinical trials across every stage of research activity. Of those, 32 studies are currently recruiting — about 29% of the sponsor's indexed portfolio — and 77 are already marked complete, representing roughly 69% of the total. 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.

The phase mix for Alcon Research reports 27 late-stage studies (Phase 3 and Phase 4 combined) and 34 earlier-phase studies (Phase 1 and Phase 2). 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.

The top therapeutic focus area indexed for Alcon Research is Cataract with 12 linked trials, and 9 other condition areas appear in the top list above. 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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial