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Completed Phase 4 Interventional Results available

Rocklatan® Evaluation

ClinicalTrials.gov ID: NCT05283395

Public ClinicalTrials.gov record NCT05283395. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 8:17 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Open-Label Rocklatan® (Netarsudil/Latanoprost Ophthalmic Solution) 0.02%/0.005% Evaluation of IOP Lowering Efficacy and Safety as Replacement of Current Medical Therapy Regimen for the Reduction of Elevated Intraocular Pressure in Patients With Glaucoma or Ocular Hypertension

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this study is to evaluate the IOP-lowering effect when subjects are switched from various latanoprost-based regimens to Rocklatan. Subjects will stop their IOP-lowering medical therapy regimen and dose with Rocklatan for the duration of the study (12 weeks).

Study identification

NCT ID
NCT05283395
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Aerie Pharmaceuticals
Industry
Enrollment
136 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 28, 2022 (Actual)
Primary completion
Mar 22, 2023 (Actual)
Completion
Mar 22, 2023 (Actual)
Last update posted
Apr 3, 2024

2022 – 2023

United States locations

U.S. sites
21
U.S. states
11
U.S. cities
20
Facility City State ZIP Site status
North Valley Eye Medical Group Mission Hills California 91345 —
Visionary Eye Institute Newport Beach California 92663 —
California Eye Specialists Medical Group Pasadena California 91107 —
North Bay Eye Associates Petaluma California 94954 —
Shettle Eye Research Largo Florida 33773 —
Center For Sight Venice Florida 34285 —
Georgia Eye Partners Atlanta Georgia 30342 —
Coastal Research Associates LLC Roswell Georgia 30076 —
Tekwani Vision Center St Louis Missouri 63128 —
OCLI Vision Manhasset New York 11030 —
Mark J. Weiss, MD, Inc. Tulsa Oklahoma 74104 —
Scott & Christie and Associates, PC Cranberry Township Pennsylvania 16066 —
Advancing Vision Research Goodlettsville Tennessee 37072 —
VRF Eye Specialty Group Memphis Tennessee 38120 —
Total Eye Care, PA Memphis Tennessee 38199 —
Keystone Research Austin Texas 78731 —
Louis M. Alpern, M.D., M.P.H., P.A El Paso Texas 79902 —
Houston Eye Associates Houston Texas 77025 —
Emerson Clinical Research Institute Falls Church Virginia 22046 —
Vistar Eye Center Roanoke Virginia 24016 —
The Eye Centers of Racine and Kenosha Racine Wisconsin 53405 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05283395, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 3, 2024 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05283395 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →