Apremilast in the Treatment of Uveitis

NCT00889421 · Status: TERMINATED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 3

Last updated 2014-07-08

Study results available
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Summary

The purpose of this study is to assess the safety and efficacy of Apremilast in the treatment of uveitis.

Conditions

  • Uveitis

Interventions

DRUG

Apremilast

oral dose of 30 mg BID for 6 months

Sponsors & Collaborators

  • Oregon Health and Science University

    lead OTHER
  • Celgene Corporation

    collaborator INDUSTRY

Principal Investigators

  • Eric B Suhler, MD, MPH · Oregon Health and Science University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-11-30
Primary Completion
2011-06-30
Completion
2011-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00889421 on ClinicalTrials.gov