Clinical Research Directory

Inclusion Criteria: 1. Be 18 years or older on the date the ICF is signed 2. Have the capacity to read, understand, and provide written voluntary informed consent 3. Have physiologically normal anterior segments not exhibiting clinically significant biomicroscopy findings 4. Have no active ocular disease or allergic conjunctivitis 5. Not be using any topical ocular medications 6. Be willing and able to follow instructions 7. Have signed a statement of informed consent 8. Be an experienced soft contact lens wearer (have previously used soft contact lenses) 9. Meet the indications per the Instructions for Use (IFU) and have a suitable prescription for treatment with the device Exclusion Criteria: 1. Is participating in another research study 2. Is considered by the Investigator to not be a suitable candidate for participation 3. Is not eligible for treatment with the study lens per the IFU (contraindicated) 4. Has had previous ocular surgery 5. Is taking/using ocular, systemic, or topical medications that, in the Investigator's opinion, could potentially affect ocular physiology or lens/solution performance