Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Novartis Pharmaceuticals
Age
18–any
Sex
MALE
Healthy volunteers
Not accepted
You may be eligible if
Females must be post-menopausal or surgically sterile, or must use concomitantly two acceptable forms of effective contraception
Clinical diagnosis of POAG or OH
For study eyes not previously treated with anti-glaucoma medications
* IOP must be ≥ 22 mm Hg at least at two assessment time-points at Screening, and
* IOP must be ≥ 22 mm Hg at least at two assessment time-points at Baseline, and
* IOP must be ≥ 20 mm Hg and ≤ 36 mm Hg at all Screening and Baseline assessment time-points.
Or for study eyes previously treated with anti-glaucoma medications
* IOP must be ≥ 14 mm Hg and ≤ 24 mm Hg at least at two assessment time-points at Screening.
* IOP must be ≥ 22 mm Hg at least at two assessment time-points at Baseline (after wash-out)
* IOP must be ≥ 20 mm Hg and ≤ 36 mm Hg at all Baseline assessment time-points
You may not be if
History of or current clinically significant ocular conditions in either eye that would contraindicate the use of an investigational drug or latanoprost (e.g. active intraocular inflammation), or that might affect interpretation of the results of the study.
History or presence of clinically significant medical problems that contraindicate the use of an investigational drug or latanoprost, including but not limited to:
* Uncontrolled hypertension with systolic blood pressure ≥ 160 mm Hg and/or diastolic blood pressure ≥ 100 mm Hg measured at more than one blood pressure reading at Screening or Baseline;
* myocardial infarction within the 3 months period prior to randomization;
* active severe viral infections such as active encephalitis, meningitis, hepatitis, herpes simplex, or herpes zoster (minor viral upper respiratory infections such as colds do not require exclusion.)
Presence of moderate or severe (grade 2 or 3) conjunctival hyperemia in the study eye at Baseline Visit.
Argon laser trabeculoplasty or any prior IOP lowering surgery in the study eye.
Ocular surgery in the study eye within 3 months prior to the Screening Visit.
