Study of Rhopressa® for the Reduction of Elevated Intraocular Pressure in Patients With Glaucoma or Ocular Hypertension in a Real-world Setting

Key Inclusion Criteria:

1. Male or female subjects (aged 18 or older)

2. Subjects diagnosed with open-angle glaucoma or ocular hypertension, and determined by
the treating physician to require additional intraocular pressure (IOP)-lowering
treatment with netarsudil 0.02%.

3. Willingness to follow protocol requirements, including signed informed consent,
routine follow-up schedule, completing questionnaires and completing laboratory tests

Key Exclusion Criteria:

1. Have any active ocular disease other than glaucoma or ocular hypertension that would
interfere with study interpretation

2. Women of childbearing potential who are pregnant, nursing, or planning a pregnancy and
not using a medically acceptable form of birth control. Male subjects with a female
partner of childbearing potential must have had a prior vasectomy or agree to use an
effective method of birth control during the treatment period and for 3 months after
the subject has completed the study.

3. Known sensitivity or allergy to the study medication or components

4. Any systemic disease or clinical evidence of any condition which would make the
subject, in the opinion of the investigator, unsuitable for the study or could
potentially confound the study results

5. Concurrent participation or prior participation in any investigational drug or device
study within the last 30 days prior to the Baseline Visit