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Completed Phase 2 Interventional Results available

Safety and Efficacy of AIN457 in Noninfectious Uveitis

ClinicalTrials.gov ID: NCT00685399

Public ClinicalTrials.gov record NCT00685399. 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 21, 2026, 11:22 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

An Open-label Proof-of-concept Study With a Double-masked, Dose-ranging Component to Assess the Effects of AIN457 in Patients With Noninfectious Uveitis

Study identification

NCT ID
NCT00685399
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
76 participants

Conditions and interventions

Interventions

  • AIN457 Drug
  • AIN 457 Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 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
May 31, 2008
Primary completion
Aug 31, 2013
Completion
Aug 31, 2013
Last update posted
Jul 16, 2017

2008 – 2013

United States locations

U.S. sites
20
U.S. states
12
U.S. cities
19
Facility City State ZIP Site status
Novartis Investigative Site Beverly Hills California 90211
Novartis Investigative Site Los Angeles California 90033
Novartis Investigative Site Sacramento California 95819
Novartis Investigative Site Denver Colorado 80210
Novartis Investigative Site Golden Colorado 80401
Novartis Investigative Site Littleton Colorado 80120
Novartis Investigative Site Atlanta Georgia 30322
Novartis Investigative Site Baltimore Maryland 21201
Novartis Investigative Site Baltimore Maryland 21287
Novartis Investigative Site Cambridge Massachusetts 02142
Novartis Investigative Site Kansas City Missouri 64111
Novartis Investigative Site Teaneck New Jersey 07666
Novartis Investigative Site New York New York 10022
Novartis Investigative Site Slingerlands New York 12159
Novartis Investigative Site Durham North Carolina 27710
Novartis Investigative Site Cleveland Ohio 44195
Novartis Investigative Site Spartanburg South Carolina 29306
Novartis Investigative Site Arlington Texas 76012
Novartis Investigative Site Austin Texas 78793
Novartis Investigative Site Houston Texas 77030

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00685399, 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 Jul 16, 2017 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00685399 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →