A Study to Evaluate the Product Performance of a New Silicone Hydrogel Contact Lens

Inclusion Criteria: * Subjects must be correctable through spherocylindrical refraction to 32 letters (0.3 logMAR) or better (distance, high contrast) in each eye * Subjects must have clear central corneas and be free of any anterior segment disorders. * Subjects must be adapted lens wearers and wear a lens in each eye and each lens must be of the same manufacture and brand. * Subjects must be myopic and require lens correction from -0.25 D to -6.00 D in each eye. * Subject must wear their current lenses for a minimum of 12 hours per day at least four days per week. * Subjects must spend at least 3 hours each workday using a computer or electronic device (ie, smartphones, tablets, eReaders). * Subjects must habitually wear soft contact lens. * Subject must have no active ocular disease or allergic conjunctivitis. * Subject must not be using any topical ocular medications. * Subjects must be bothered (occasionally or frequently) by blurriness or fluctuations in vision with their current contact lenses. * Subjects must habitually use a lens care product for cleaning, disinfection, and storage. Exclusion Criteria: * Subjects who have worn gas permeable (GP) contact lenses within the last 30 days or who have worn polymethylmethacrylate (PMMA) lenses within the last three months. * Subjects with any systemic disease currently affecting ocular health or which in the Investigator's opinion may have an effect on ocular health during the course of the study. * Subjects using any systemic or topical medications that will, in the Investigator's opinion, affect ocular physiology or lens performance. * Subjects with an active ocular disease or who are using any ocular medication. * Subjects who are not correctable to 32 letters (0.3 logMAR) in each eye with soft spherical contact lenses. * Subjects who are presbyopic or currently wear monovision, multifocal, or toric contact lenses. * Subjects with an ocular astigmatism of 1.00 D or greater in either eye. * Subjects with anisometropia (spherical equivalent) of 2.00 D or greater in either eye. * Subjects with any Grade 2 or greater finding during the slit lamp examination. * Subjects with corneal infiltrates, of ANY GRADE, are not eligible. * Subjects with any "Present" finding during the slit lamp examination that, in the Investigator's judgment, interferes with contact lens wear. * Subjects with any scar or neovascularization within the central 4 mm of the cornea. * Subjects who are aphakic. * Subjects who are amblyopic. * Subjects who have had any corneal surgery (eg, refractive surgery). * Subjects who are allergic to any component in the study care products. * Subjects who are bothered by blurriness or fluctuations in vision due to itchy eyes, something on or under the lens, allergies, or cigarette smoke.