Dose Response Study of AL-37807 Ophthalmic Solution in Patients With Open-Angle Glaucoma or Ocular Hypertension

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-03-31

Brief Summary

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The purpose of thie study is to compare the safety and IOP-lowering efficacy of AL-37807 Ophthalmic Solution 0.05%, 0.1% and 0.2% dosed QD AM to Xalatan dosed QD PM and Vehicle in patients with open-angle glaucoma or ocular hypertension

Detailed Description

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Conditions

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Open-Angle Glaucoma Ocular Hypertension

Keywords

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Open-angle glaucoma ocular hypertension

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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Xalatan

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Open-angle glaucoma
* ocular hypertension

Exclusion Criteria

\- VA worse than 0.60

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Principal Investigators

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Theresa Landry

Role: STUDY_DIRECTOR

Alcon Research

Locations

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Atlanta

Atlanta, Georgia, United States

Site Status

Countries

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United States

Other Identifiers

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C-06-10

Identifier Type: -

Identifier Source: org_study_id