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Completed Phase 2 Interventional Results available

Safety and Efficacy of ENV515 Travoprost Extended Release (XR) in Patients With Bilateral Ocular Hypertension or Primary Open Angle Glaucoma

ClinicalTrials.gov ID: NCT02371746

Public ClinicalTrials.gov record NCT02371746. 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 22, 2026, 5:09 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 Multi-Center, Three-Stage, Open-Label, Prospective, Active-Comparator-Controlled Phase 2a Study of ENV515 (Travoprost) Intracameral Implant in Patients With Bilateral Ocular Hypertension or Early Primary Open-Angle Glaucoma

Brief summary

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

This is a multiple cohort study that will evaluate the safety and efficacy of ENV515 travoprost XR in patients with open-angle glaucoma or ocular hypertension.

Study identification

NCT ID
NCT02371746
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Envisia Therapeutics
Industry
Enrollment
41 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 85 Years
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
Jan 1, 2015 (Actual)
Primary completion
Feb 13, 2019 (Actual)
Completion
Feb 13, 2019 (Actual)
Last update posted
Oct 17, 2019

2015 – 2019

United States locations

U.S. sites
14
U.S. states
9
U.S. cities
14
Facility City State ZIP Site status
Not listed Chandler Arizona 85225 —
Not listed Garden Grove California 92843 —
Not listed Inglewood California 90301 —
Not listed Redding California 96002 —
Not listed Morrow Georgia 30260 —
Not listed Indianapolis Indiana 46260 —
Not listed Chesterfield Missouri 63017 —
Not listed Kansas City Missouri 64133 —
Not listed Cincinnati Ohio 45242 —
Not listed Portland Oregon 97210 —
Not listed Sioux Falls South Dakota 57108 —
Not listed Austin Texas 78731 —
Not listed Houston Texas 77025 —
Not listed San Antonio Texas 78229 —

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 NCT02371746, 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 Oct 17, 2019 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02371746 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →