Subject Population. The study population for Part A and Part B each includes approximately 66 volunteer subjects to be enrolled at approximately 4 sites, with approximately 16-18 subjects enrolled per site. The study population will consist of subjects with normal eyes (other than the need for optical correction for myopia), who are adapted, existing wearers of soft contact lenses in both eyes.
Appears in 1 contract
Samples: Investigator Agreement
Subject Population. The study population for Part A and Part B each includes approximately 66 48 volunteer subjects to be enrolled at approximately 4 3 sites, with approximately 16-18 16 subjects enrolled per site. The study population will consist of subjects with normal eyes (other than the need for optical correction for myopiarefractive ametropia), who are adapted, existing wearers of soft frequent replacement daily wear contact lenses in both eyes. ,
Appears in 1 contract
Samples: Investigator Agreement
Subject Population. The study population for Part A and Part B each includes approximately 66 22 volunteer subjects to be enrolled at approximately 4 sites, with approximately 16-18 subjects enrolled per 1 site. The study population will consist of subjects with normal eyes (other than the need for optical correction for myopia), and who are adapted, existing wearers of daily disposable soft contact lenses in both eyes. Subjects must be screened according to the full list of inclusion/exclusion criteria in Section 1 of this protocol. Rescreening of subjects is not allowed in this study.
Appears in 1 contract
Samples: clinicaltrials.gov
Subject Population. The study population for Part A and Part B each includes approximately 66 36 volunteer subjects to be enrolled at approximately 4 3 sites, with approximately 16-18 12 subjects enrolled per site. The study population will consist of subjects with normal eyes (other than the need for optical correction for myopiarefractive ametropia), who are adapted, existing wearers of soft weekly/monthly contact lenses in both eyes. , Rescreening of subjects after screen failure is not allowed in this study.
Appears in 1 contract
Samples: Investigator Agreement
Subject Population. The study population for Part A and Part B each includes approximately 66 volunteer subjects to be enrolled at approximately 4 3 sites, with approximately 16-18 22 subjects enrolled per site. The study population will consist of subjects with normal eyes (other than the need for optical correction for myopia), and who are adapted, existing wearers of daily disposable soft contact lenses in both eyes. Subjects must be screened according to the full list of inclusion/exclusion criteria in Section 1 of this protocol. Rescreening of subjects is not allowed in this study.
Appears in 1 contract
Samples: classic.clinicaltrials.gov
Subject Population. The study population for Part A and Part B each includes approximately 66 36 volunteer subjects to be enrolled at approximately 4 2 sites, with approximately 1618-18 36 subjects enrolled per site. The study population will consist of subjects with normal eyes (other than the need for optical correction for myopia), refractive ametropia) and who are adapted, existing wearers of soft contact lenses in both eyes. Subjects must be screened according to the full list of inclusion/exclusion criteria in Section 1 of this protocol. Rescreening of subjects after screen failure is not allowed in this study.
Appears in 1 contract
Samples: Investigator Agreement