CooperVision International Limited (CVIL)
CooperVision International Limited (CVIL) sponsors 11 registered US clinical trials on ClinicalTrials.gov, 4 of them currently recruiting, and 5 completed. The most-studied condition in this pipeline is Myopia, with 3 trials.
Trial Pipeline
11 total, page 1 of 1
Performance of Two Daily Disposable Multifocal Contact Lenses
NCT07444658
Comprehensive Assessment of Multiple Products (CAMP)
NCT07276347
A Clinical Comparison of Proclear® 1 Day Multifocal and Clariti® 1 Day Multifocal 3 Add
NCT06869044
North American Comfilcon A Clinical Study
NCT06902584
Contact Lens Trial Fitting Experience
NCT07600645
Optimization for Toric Contact Lenses
NCT07557030
Performance Comparison of Two Monthly Replacement Silicone Hydrogel Multifocal Lens Types
NCT06232590
Clinical Evaluation of Reusable Soft Contact Lenses
NCT06119191
Performance Evaluation of Two Silicone Hydrogel Toric Lens Designs in Habitual Soft Contact Lens Wearers
NCT05933772
Corneal Refractive Therapy Design Comparison for -4 to -6 Diopter Treatment for Overnight Wear for Myopia
NCT05438615
High Refractive Index Material 510(k)
NCT00766168
Therapeutic Areas
What the Pipeline for CooperVision International Limited (CVIL) Shows
According to the ClinicalTrials.gov registry, CooperVision International Limited (CVIL) is linked to 11 US clinical trials across every stage of research activity. Of those, 4 studies are currently recruiting, about 36% of the sponsor's indexed portfolio, and 5 are already marked complete, representing roughly 45% of the total.
The phase mix for CooperVision International Limited (CVIL) 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 International Limited (CVIL) is Myopia with 3 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.