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ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional

A Study of Brepocitinib in Adults With Active, Non-Infectious, Non-Anterior Uveitis

ClinicalTrials.gov ID: NCT06431373

Public ClinicalTrials.gov record NCT06431373. 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 Oct 22, 2026, 1:37 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

A Phase 3 Randomized, Double-Masked, Placebo-Controlled Study to Investigate the Safety and Efficacy of Oral Brepocitinib in Adults With Active, Non-Infectious Intermediate-, Posterior-, and Panuveitis

Brief summary

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

The purpose of this study is to determine the safety and efficacy of brepocitinib in participants with active, non-anterior (intermediate, posterior, or pan) non-infectious uveitis (NIU).

Study identification

NCT ID
NCT06431373
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Priovant Therapeutics, Inc.
Industry
Enrollment
371 participants

Conditions and interventions

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
Sep 11, 2024 (Actual)
Primary completion
Sep 11, 2026 (Estimated)
Completion
Feb 1, 2028 (Estimated)
Last update posted
Jan 12, 2026

2024 – 2028

United States locations

U.S. sites
53
U.S. states
23
U.S. cities
47
Facility City State ZIP Site status
Clinical Trial Site Phoenix Arizona 85020 —
Clinical Trial Site Phoenix Arizona 85054 —
Clinical Trial Site Bakersfield California 93309 —
Clinical Trial Site Beverly Hills California 90211 —
Clinical Trial Site Fullerton California 92835 —
Clinical Trial Site Irvine California 92697 —
Clinical Trial Site La Jolla California 92093 —
Clinical Trial Site Los Angeles California 90033 —
Clinical Trial Site Los Angeles California 90095 —
Clinical Trial Site Modesto California 95356 —
Clinical Trial Site Sacramento California 92825 —
Clinical Trial Site Aurora Colorado 80045 —
Clinical Trial Site Denver Colorado 80246 —
Clinical Trial Site Fort Lauderdale Florida 33308 —
Clinical Trial Site St. Petersburg Florida 33711 —
Clinical Trial Site Chicago Illinois 60637 —
Clinical Trial Site Oak Park Illinois 60304 —
Clinical Trial Site Carmel Indiana 46290 —
Clinical Trial Site Prairie Village Kansas 66208 —
Clinical Trial Site Baltimore Maryland 21287 —
Clinical Trial Site Boston Massachusetts 02114 —
Clinical Trial Site Waltham Massachusetts 02451 —
Clinical Trial Site Ann Arbor Michigan 48105 —
Clinical Trial Site Detroit Michigan 48201 —
Clinical Trial Site Detroit Michigan 48202 —
Clinical Trial Site Minneapolis Minnesota 55455 —
Clinical Trial Site Rochester Minnesota 55905 —
Clinical Trial Site St Louis Missouri 63108 —
Clinical Trial Site Omaha Nebraska 68105 —
Clinical Trial Site Palisades Park New Jersey 07650 —
NYU Langone Health New York New York 10017 —
Clinical Trial Site Rochester New York 14642 —
Clinical Trial Site Durham North Carolina 27705 —
Clinical Trial Site Winston-Salem North Carolina 27157 —
Clinical Trial Site Cleveland Ohio 44106 —
Clinical Trial Site Cleveland Ohio 44195 —
Clinical Trial Site Columbus Ohio 43212 —
Clinical Trial Site Portland Oregon 97221 —
Clinical Trial Site Portland Oregon 97239 —
Clinical Trial Site Erie Pennsylvania 16507 —
Clinical Trial Site Philadelphia Pennsylvania 19107 —
Clinical Trial Site Philadelphia Pennsylvania 19141 —
Clinical Trial Site Greenville South Carolina 29605 —
Clinical Trial Site Nashville Tennessee 37232 —
Clinical Trial Site Austin Texas 78712 —
Clinical Trial Site Bellaire Texas 77401 —
Clinical Trial Site Dallas Texas 75390 —
Clinical Trial Site Houston Texas 77025 —
Clinical Trial Site Katy Texas 77494 —
Clinical Trial Site Plano Texas 75075 —
Clinical Trial Site Round Rock Texas 78681 —
Clinical Trial Site San Antonio Texas 78230 —
Clinical Trial Site Madison Wisconsin 53705 —

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 54 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06431373, 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 Jan 12, 2026 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06431373 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →