Clinical Performance of a Silicone Hydrogel Contact Lens Following Six Nights of Extended Wear

Clinical Performance of a Silicone Hydrogel Following Six Nights of Extended Wear

The purpose of this clinical study is to evaluate the on-eye performance of an investigational soft contact lens compared to a commercially available soft contact lens following 1 week of extended wear.

Subjects will be randomized to wear the investigational contact lens in 1 eye and the commercially available contact lens in the other eye. Subjects will be expected to attend 3 scheduled study visits: Day 1 Baseline/Dispense; Day 2 Follow-up; and Week 1 Follow-up/Exit. The expected duration of exposure to each of the study lenses for all randomized, completed subjects was approximately 7 days / 6 nights of wear.

Key Inclusion Criteria:

• Able to understand and sign an Institutional Review Board/Ethics Committee-approved Informed Consent form.
• Successful wear of spherical soft contact lenses in both eyes during the past 3 months for a minimum of 5 days per week and in an extended wear modality a minimum of 1 night per week.
• Best Corrected Visual Acuity (BCVA) of 20/25 or better in each eye.
• Other protocol-specified inclusion criteria may apply.

Key Exclusion Criteria:

• Any condition, use of medications, or surgery that could contraindicate contact lens wear, as determined by the Investigator.
• Current Biofinity© lens wearer.
• Pregnant or breast-feeding.
• Other protocol-specified exclusion criteria may apply.