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Clinical trialNCT03828019CompletedPhase 3Interventional

Adalimumab vs. Conventional Immunosuppression for Uveitis Trial

SponsorJHSPH Center for Clinical TrialsEnrollment227Uveitis
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Non-infectious intermediate, posterior, and panuveitides are chronic, potentially-blinding diseases. Vision-threatening cases require long-term therapy with oral corticosteroids and immunosuppression. Based upon preliminary data, adalimumab, a fully-human, anti-tumor necrosis(TNF)-α monoclonal antibody, now US FDA-approved for uveitis treatment, may be a superior corticosteroid-sparing agent than conventional immunosuppressive drugs. The ADVISE Trial is multicenter randomized, parallel-treatment, comparative effectiveness trial comparing adalimumab to conventional (small molecule) immunosuppression for corticosteroid spring in the treatment of non-infectious, intermediate, posterior, and panuveitides.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

26 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Australia
  • Centre for Eye Research Australia

    East Melbourne, Victoria, Australia

  • University of Sydney

    Sydney, Australia

United Kingdom
  • University Hospital Birmingham

    Edgbaston, Birmingham, United Kingdom

  • Bradford Teaching Hospital Nhs Foundation Trust

    Bradford, United Kingdom

  • Cambridge University Nhs Trust

    Cambridge, United Kingdom

  • University Hospitals of Leicester

    Leicester, United Kingdom

  • Moorfields Eye Hospital Nhs Foundation Trust

    London, United Kingdom

United States
  • Jules Stein Eye Institute, Ucla

    Los Angeles, California, United States

  • University of California, San Francisco

    San Francisco, California, United States

  • Anne Bates Leach Eye Hospital, University of Miami Miller School of Medicine

    Miami, Florida, United States

  • Emory University

    Atlanta, Georgia, United States

  • Northwestern University

    Chicago, Illinois, United States

  • Rush University Medical Center

    Chicago, Illinois, United States

  • University of Iowa

    Iowa City, Iowa, United States

  • Johns Hopkins University

    Baltimore, Maryland, United States

  • National Eye Institute

    Bethesda, Maryland, United States

  • Ophthalmic Consultants of Boston

    Boston, Massachusetts, United States

  • University of Michigan Health System, Kellogg Eye Center

    Ann Arbor, Michigan, United States

  • Washington University

    St Louis, Missouri, United States

  • Midatlantic Retina, Wills Eye Hospital

    Philadelphia, Pennsylvania, United States

  • University of Pittsburgh Medical Center

    Pittsburgh, Pennsylvania, United States

  • Tennessee Retina

    Nashville, Tennessee, United States

  • Vanderbilt University Eye Institute

    Nashville, Tennessee, United States

  • Retinal Consultants of Texas

    Bellaire, Texas, United States

  • University of Utah, Moran Eye Center

    Salt Lake City, Utah, United States

  • University of Washington, Medicine Eye Institute

    Seattle, Washington, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Adalimumab →Conventional immunosuppression
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
16 Sept 2019
Primary completion
2 Apr 2024
Completion
9 Sept 2024
Last update posted
16 May 2025
Registered enrollment
227
Registry id
NCT03828019

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.