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Completed Phase 2 Interventional Results available

Study to Assess the Efficacy, Safety and Tolerability of AKB-9778 Ophthalmic Solution as and Adjunct to Latanoprost in Patients With Ocular Hypertension or Open Angle Glaucoma

ClinicalTrials.gov ID: NCT04405245

Public ClinicalTrials.gov record NCT04405245. 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 Jul 23, 2026, 5:58 PM EDT

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

Official title

Phase 2 Multi-Center, Double-Masked, Randomized, 28-Day Study to Assess the Efficacy, Safety and Tolerability of Single or Twice Daily Doses of AKB-9778 Ophthalmic Solution as an Adjunct to Latanoprost in Patients With Ocular Hypertension (OHT) or Open Angle Glaucoma (OAG)

Study identification

NCT ID
NCT04405245
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
EyePoint Pharmaceuticals, Inc.
Industry
Enrollment
194 participants

Conditions and interventions

Interventions

  • Latanoprost ophthalmic solution Drug
  • AKB-9778 4% Drug
  • Placebo Drug

Drug

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
Jun 5, 2020
Primary completion
Nov 4, 2020
Completion
Nov 4, 2020
Last update posted
May 24, 2023

2020

United States locations

U.S. sites
21
U.S. states
12
U.S. cities
21
Facility City State ZIP Site status
United Medical Research Institute Inglewood California 90301
North Valley Eye Medical Group Mission Hills California 91345
Eye Research Foundation Newport Beach California 92663
North Bay Eye Associates Petaluma California 94954
Shettle Eye Research Largo Florida 33773
Clayton Eye Clinical Research, LLC Morrow Georgia 30260
Coastal Research Associates Roswell Georgia 30076
Kannarr Eye Care Pittsburg Kansas 66762
Heart of America Eye Care, P.A. Shawnee Mission Kansas 66204
Tekwani Vision Center St Louis Missouri 63128
North Valley Eye Medical Group Rochester New York 14618
Charlotte Eye, Ear, Nose & Throat Assoc. (CEENTA) Charlotte North Carolina 28210
James D. Branch, MD Ophthalmology Winston-Salem North Carolina 27101
Apex Eye Cincinnati Ohio 45242
Abrams Eye Center Cleveland Ohio 44115
Mark J. Weiss, MD, Inc. Tulsa Oklahoma 74104
Scott & Christie and Assoc Cranberry Township Pennsylvania 16066
Eye Care Specialists Kingston Pennsylvania 18704
Total Eye Care Memphis Tennessee 38119
Advancing Vision Research Nashville Tennessee 37205
Texan Eye / Keystone Research Austin Texas 78731

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 NCT04405245, 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 May 24, 2023 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04405245 live on ClinicalTrials.gov.

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