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Completed Phase 1Phase 2 Interventional

Efficacy, Tolerability and Safety of RKI983 (0.05% & 0.10%) vs Xalatan in Patients With POAG or Ocular Hypertension

ClinicalTrials.gov ID: NCT00846989

Public ClinicalTrials.gov record NCT00846989. 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 Nov 11, 2026, 5:32 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 4-week Multi-center, Single-masked, Randomized, Latanoprost-controlled, Parallel Group Study to Assess the Efficacy, Tolerability and Safety of RKI983 (0.05% and 0.10%) Ophthalmic Solution Given Twice a Day Versus Once Daily Latanoprost 0.005%, in Patients With Primary Open Angle Glaucoma or Ocular Hypertension.

Brief summary

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

This purpose of this study is to access the efficacy, tolerability and safety of RKI983 (0.05% and 0.10%) ophthalmic solution bid versus once daily latanoprost 0.005%, in patients with POAG or ocular hypertension.

Study identification

NCT ID
NCT00846989
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
276 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
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 2009 (Type not available)
Primary completion
Apr 2009 (Actual)
Completion
Apr 2009 (Actual)
Last update posted
Dec 19, 2020

2009

United States locations

U.S. sites
29
U.S. states
18
U.S. cities
28
Facility City State ZIP Site status
Novartis Investigative Site Artesia California 90701 —
Novartis Investigative Site Inglewood California 90301 —
Novartis Investigative Site La Jolla California 92037 —
Novartis Investigative Site Poway California 92064 —
Novartis Investigative Site Stockton California 95207 —
Novartis Investigative Site Danbury Connecticut 06810 —
Novartis Investigative Site Atlanta Georgia 30342 —
Novartis Investigative Site Morrow Georgia 30260 —
Novartis Investigative Site Roswell Georgia 30076 —
Novartis Investigative Site Kaneohe Hawaii 96744 —
Novartis Investigative Site Topeka Kansas 66606 —
Novartis Investigative Site Louisville Kentucky 40217 —
Novartis Investigative Site Bossier City Louisiana 71111 —
Novartis Investigative Site Cambridge Massachusetts 02142 —
Novartis Investigative Site Springfield Missouri 65804 —
Novartis Investigative Site Omaha Nebraska 68131 —
Novartis Investigative Site Las Vegas Nevada 89148 —
Novartis Investigative Site Bethpage New York 11714 —
Novartis Investigative Site Lynbrook New York 11563 —
Novartis Investigative Site Rochester New York 14618 —
Novartis Investigative Site Charlotte North Carolina 28204 —
Novartis Investigative Site Charlotte North Carolina 28210 —
Novartis Investigative Site Tulsa Oklahoma 74104 —
Novartis Investigative Site Mt. Pleasant South Carolina 29464 —
Novartis Investigative Site Memphis Tennessee 38119 —
Novartis Investigative Site El Paso Texas 79904 —
Novartis Investigative Site Houston Texas 77030 —
Novartis Investigative Site San Antonio Texas 78229 —
Novartis Investigative Site Spokane Washington 99202 —

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 NCT00846989, 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 Dec 19, 2020 · Synced Nov 11, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00846989 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →