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 2 of 2
Multi-center Clinical Evaluation of PC 1-Day vs 1-Day Acuvue Moist
NCT02024698
Clinical Evaluation of Hydrogels vs Silicone Hydrogel Contact Lenses
NCT01966770
Multicenter Dispensing Study of Biofinity Lenses in Extended Range
NCT02060539
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
NCT01952665
Evaluation of Comfilcon A and Senofilcon A Lenses
NCT01695369
Evaluation of Enfilcon A Soft Contact Lens When Compared to Galyfilcon A Soft Contact Lens
NCT01706770
Comparative Study of Two Marketed Spherical Soft Contact Lenses
NCT01582789
Clinical Comfort Evaluation of Two Marketed Spherical Contact Lenses
NCT02356692
Proclear 1-D Multifocal Nondispensing Study
NCT01526902
Comparative Study of Two Marketed 1-day Soft Contact Lenses
NCT01464255
Evaluation of DW Silicone Hydrogel Lens Compared to DW Silicone Hydrogel Lens
NCT01386008
Clinical Evaluation of Stenfilcon A Soft Contact Lens When Compared to Ocufilcon B Soft Contact Lens
NCT01354223
A Clinical Comparison of Marketed Lens Care Solutions With Avaira Lens Brand
NCT01335750
Study of Soft Contact Lens Use With 7 Day Extended Wear
NCT00597467
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.