CooperVision
CooperVision sponsors 64 registered US clinical trials on ClinicalTrials.gov, 2 of them currently recruiting, and 61 completed. The most-studied condition in this pipeline is Myopia, with 13 trials.
Trial Pipeline
64 total, page 1 of 2
MiSight 1 Day Safety Post-Approval Study
NCT05285527
MiSight 1 Day Post-Approval Study for Effectiveness and Visual Symptoms
NCT05285553
1 Week Crossover Study Between Two Soft Contact Lenses
NCT06611410
Performance Evaluation of Reusable Contact Lenses When Worn For One Month By Habitual Soft Contact Lens Wearers
NCT06098339
Performance Evaluation of Different Daily Disposable Silicone Hydrogel Contact Lenses
NCT05805059
Performance Evaluation of Daily Disposable Contact Lenses in Habitual Lens Wearers Who Use Digital Devices Frequently
NCT05805150
Performance Evaluation of Different Daily Disposable Multifocal Contact Lenses
NCT05763628
Evaluating Two Multifocal Daily Disposable Contact Lenses
NCT05579886
Evaluation of Monthly Replacement Lenses in Habitual Soft Contact Lens Wearers Who Report Frequent Digital Devise Use
NCT05166902
Evaluation of the Performance of Monthly Replacement Sphere Lens Designs in Habitual Soft Contact Lens Wearers
NCT05114564
Evaluating the Success of Habitual Multifocal Wearers When Refit With a New Lens Design
NCT04952701
Clinical Validation of the Apollo Daily Disposable Soft Contact Lenses
NCT05035017
Performance Evaluation of Two Daily Disposable Toric Lens Designs in Habitual Soft Contact Lens Wearers
NCT04831515
Evaluation of the Performance of Different Daily Disposable Lens Designs in Habitual Soft Contact Lens Wearers
NCT04668989
A Two-Week Crossover Dispensing Evaluation Of Orion Daily Wear Soft Contact Lens
NCT04585646
Comparing Biofinity Toric Multifocal to Ultra Multifocal for Astigmatism
NCT04404725
Comparing the Performance of 1 Day Multifocal Contact Lenses
NCT04449263
Evaluation Of One Silicone Hydrogel Contact Lens and Two Hydrogel Lenses in Daily Wear
NCT04050618
Clinical Evaluation of Invigor Toric 1-Day Contact Lenses
NCT04016623
A Dispensing Comparison of a Test Daily 1 Day Lens Against a Control 1 Day Lens.
NCT03951610
Comparison of Two Daily Disposable Soft Contact Lenses
NCT03779503
Evaluation of Silicone Hydrogel Daily Wear Contact Lenses for Up to One (1) Month of Daily Wear
NCT03722784
Performance of Wearers of Stenfilcon A Contact Lenses After A Refit With Test Lenses
NCT03496701
A Dispensing Clinical Trial of Test Contact Lens Against Marketed Contact Lens
NCT03499067
Clinical Validation Study of Comfilcon A Multifocal Toric Contact Lenses
NCT03417557
Comparison of New Contact Lens With Current Marketed Lens
NCT03360110
A One-Week Crossover Dispensing Evaluation of New Daily Wear Soft Contact Lenses
NCT03306641
A 6-Hour Clinical Evaluation of New Daily-Wear Soft Contact Lenses
NCT03235089
Daily Disposable Dispensing Clinical Trial of Test Lens Against Stenfilcon A Lens
NCT03024970
Performance Comparison Between Fanfilcon A and Senofilcon A Sphere Lenses
NCT02956460
Performance of Fanfilcon A Toric Lenses After at Least One Month Wearing Enfilcon A Toric Lenses
NCT02921412
Performance Comparison Between Comfilcon A and Senofilcon C Lenses
NCT02920957
One Month Dispensing Study Comparing the Clinical Performance of the Comfilcon A Sphere Lenses Compared to Comfilcon A Asphere Lenses.
NCT02759471
A Dispensing Clinical Trial of Comfilcon A Extended Range Multifocal Lenses
NCT02719353
A Dispensing Clinical Trial of Comfilcon A Extended Range Multifocal Lenses
NCT02719366
Dispensing Study for a New Study Lens
NCT02642991
Evaluation of the CooperVision, Inc. Fanfilcon A and Enfilcon A Daily Wear Contact Lenses When Used for Frequent Replacement for up to One (1) Month of Daily Wear
NCT02555722
A Bilateral Dispensing Clinical Trial of an Sapphire Lens Against Senofilcon A Toric for Astigmatism Lens
NCT02555098
Bilateral Dispensing Study of Fanfilcon A Toric Versus Enfilcon A Toric Lenses
NCT02423109
One Week Assessment of The Phenacite Lens
NCT02553395
A Contralateral Dispensing Clinical Trial of Study Test Sapphire Lens Against Enfilcon A Silicone Hydrogel Lens
NCT02518490
Multi-Center Clinical Evaluation of Two Reusable Soft Contact Lenses
NCT02542072
Bilateral Dispensing Clinical Trial of Stenfilcon A Against Etafilcon A for Astigmatism
NCT02410824
Dispensing Study for the Phenacite Project
NCT02436005
Evaluation of Investigational (Frequent Replacement) FRP Lens for Daily Wear
NCT02362724
Lens Fitting Evaluation of CooperVision MyDay™ Compared With 1-DAY ACUVUE® TruEye® and DAILIES TOTAL1®
NCT02341859
A Bilateral Dispensing Clinical Trial of Sapphire Lens Against Senofilcon A Lens Over 2 Weeks
NCT02345811
Multicenter Dispensing Study of Biofinity Toric Made-To-Order Lenses in Extended Power Ranges
NCT02193178
Clinical Validation of Biofinity Toric MTO (Made To Order) Lenses
NCT02185105
Clinical Evaluation of Daily Disposable Contact Lenses
NCT02097030
Therapeutic Areas
What the Pipeline for CooperVision Shows
According to the ClinicalTrials.gov registry, CooperVision is linked to 64 US clinical trials across every stage of research activity. Of those, 2 studies are currently recruiting, about 3% of the sponsor's indexed portfolio, and 61 are already marked complete, representing roughly 95% of the total.
The phase mix for CooperVision reports 0 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for CooperVision is Myopia with 13 linked trials, and 4 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.