Phase 3 Evaluation of the Safety and Efficacy of LNZ101 for the Treatment of Presbyopia

Phase 3 study to evaluate the safety and effectiveness of LNZ101 for the treatment of Presbyopia.

Inclusion Criteria:Be able and willing to provide written informed consent and sign a Health Information Portability and Accountability Act (HIPAA) form prior to any study procedure being performed;Be able and willing to follow all instructions and attend all study visits;Be 45-75 years of age of either sex and any race or ethnicity at Visit 1;Have +1.00 to -4.00 diopter (D) of sphere calculated in minus cylinder (so that spherical equivalent (SE) results in myopia no more severe than -4.00 D MRSE) in both eyes determined by manifest refraction documented at Visit 1;Have ≤2.00 D of cylinder (minus cylinder) in both eyes determined by manifest refraction documented at Visit 1;Be presbyopic as determined at Visit 1Exclusion Criteria:Subjects must not:Be a female of childbearing potential who is currently pregnant, nursing, or planning a pregnancy;Have known contraindications or sensitivity to the use of any of the study medications or their components;Have an active ocular infection at Visit 1 or at Visit 2 (bacterial, viral, or fungal), positive history of an ocular herpetic infection, preauricular lymphadenopathy, or ongoing, active ocular inflammation in either eye;Have moderate or severe dry eye defined as total central corneal fluorescein staining in either eye at Visit 1;Have clinically significant abnormal lens findings including early lens changes in either eye during dilated slit-lamp biomicroscopy and fundus exam documented within 3 months of Visit 1 or at Visit 1;