Phase 4
Completed N=260
Study of Rhopressa® for the Reduction of Elevated Intraocular Pressure in Patients With Glaucoma or Ocular Hypertension in a Real-world Setting
Glaucoma, Open-Angle · Hypertension
Source: ClinicalTrials.gov NCT03808688 ↗
Enrolled (actual)
260
Serious AEs
1.2%
Results posted
Sep 2020
Primary outcomePrimary: Intraocular Pressure (IOP) — -16.9; -2.3; 0.2; -17.0 percent change
◆ Published Evidence
Emerging
19citations · ~4 / year
A multicenter, open-label study of netarsudil for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension in a real-world setting.
Summary
To evaluate the IOP lowering efficacy of netarsudil ophthalmic solution 0.02% when used as monotherapy or when used concomitantly with other IOP-lowering agents in subjects with elevated IOP due to open angle glaucoma or ocular hypertension in a real-world clinical setting. The study is an open-label design. The patients will receive treatment for 12 weeks.
Linked Publications
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A multicenter, open-label study of netarsudil for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension in a real-world setting.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Intraocular Pressure (IOP) |
-16.9; -2.3; 0.2; -17.0 | — |
Eligibility Criteria
Key Inclusion Criteria
- Male or female subjects (aged 18 or older)
- 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%.
- Willingness to follow protocol requirements, including signed informed consent, routine follow-up schedule, completing questionnaires and completing laboratory tests
Key Exclusion Criteria
- Have any active ocular disease other than glaucoma or ocular hypertension that would interfere with study interpretation
- 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.
- Known sensitivity or allergy to the study medication or components
- 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
- Concurrent participation or prior participation in any investigational drug or device study within the last 30 days prior to the Baseline Visit
Data sourced from ClinicalTrials.gov (NCT03808688) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.