Clinical Comparison of Two Daily Disposable Silicone Hydrogel Soft Contact Lens

Inclusion Criteria: * Subject should have normal eyes and use no ocular medications * Subject with -1.00 to -10.00 D myopia, less than 2.00 D astigmatism * VA correctable to Log MAR 0.1 or better. * Willing to comply with all study procedures and be available for the duration of the study. * Provide signed and dated informed consent form. Exclusion Criteria: * Subjects have history of allergies that would contraindicate "normal" contact lens wear. * Subjects have other active ocular or systemic disease such as, but not limited to : anterior uveitis (past or present), glaucoma, Sjögren's syndrome, lupus erythematosus, sclerodermas, keratoconus or type II diabetes. * Subjects have medications that would contraindicate contact lens wear. * Currently pregnant (to the best of the subject's knowledge), is lactating or is planning a pregnancy within the next 3 month. * Current drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements. * Any active participation in another clinical trial within 30 days prior to this study. * The presence of clinically significant (grade 3 or 4) anterior segment abnormalities; inflammations such as iritis; or any infection of the eye, lids, or associated structures. * A known history of corneal hypoesthesia (reduced corneal sensitivity), corneal ulcer, corneal infiltrates or fungal infections. * A history of papillary conjunctivitis that has interfered with contact lens wear.