ClinicalTrials.gg
Active, not recruitingNCT06431373CLARITYUpdated Jan 12, 2026

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

A Phase 3 interventional study of Brepocitinib PO QD and Placebo PO QD in Uveitis, Posterior, Uveitis, Intermediate and Uveitis, sponsored by Priovant Therapeutics, Inc.. Active, not recruiting at 107 sites in 13 countries. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-01-12.

Sponsored by Priovant Therapeutics, Inc. · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
371
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

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).

02

Conditions studied

  • Uveitis, Posterior
  • Uveitis, Intermediate
  • Uveitis
03

In context

Uveitis, Posterior

61 studies on the registry are indexed under Uveitis, Posterior; 4 are open to participants now.

This study's enrollment of 371 is above the median of 37 across 45 interventional studies indexed under Uveitis, Posterior.

Browse Uveitis, Posterior studies →

Lead sponsor

Priovant Therapeutics, Inc. is the lead sponsor of 6 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult subjects (18-75 years old)
  • Diagnosis of non-infectious uveitis (intermediate uveitis, posterior uveitis, or panuveitis)
  • Active uveitic disease in at least 1 eye
  • Weight > 40 kg with a ≤ 40 kg/m2

Exclusion criteria

Exclusion Criteria:

Has confirmed or suspected current diagnosis of infectious uveitis History of or have:

  1. Lymphoproliferative disorder
  2. active
  3. cancer within 5 years prior to screening (exceptions for basal cell carcinoma, squamous cell carcinoma, ductal carcinoma in situ of the breast, carcinoma in situ of the uterine cervix, or thyroid carcinoma.)
  4. thrombosis or cerebrovascular ischemic event disease within the last 12 months
  5. a high risk for herpes zoster reactivation
  6. active or recent infections
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
371 participants (actual)

Study arms

  • Experimental
    Arm 1

    Drug: Brepocitinib PO QD

  • Placebo comparator
    Arm 2

    Drug: Placebo PO QD

Interventions

  • DrugBrepocitinib PO QD

    Brepocitinib PO QD

  • DrugPlacebo PO QD

    Placebo PO QD

06

What researchers measure

Primary outcomes

  1. Time to treatment failure on or after Period 1 Week 6 up to Period 1 Week 48

    Time frame: 48 weeks

Secondary outcomes

  1. Proportion of participants meeting treatment failure criteria on or after Period 1 Week 6 up to Period 1 Week 24

    Time frame: 24 weeks

  2. Change in logMAR BCVA in each eye from best state achieved at or prior to Period 1 Week 6 up to Period 1 Week 24

    Time frame: 24 weeks

  3. Change in central subfield thickness from best state achieved in each eye at or prior to Period 1 Week 6 up to Period 1 Week 24

    Time frame: 24 weeks

  4. Change in logMAR BCVA in each eye from best state achieved at or prior to Period 1 Week 6 up to Period 1 Week 48

    Time frame: 48 Weeks

  5. Change in central subfield thickness from best state achieved in each eye at or prior to Period 1 Week 6 up to Period 1 Week 48

    Time frame: 48 weeks

07

Study locations

107 sites
  • Clinical Trial Site
    Phoenix, Arizona 85020, United States
  • Clinical Trial Site
    Phoenix, Arizona 85054, United States
  • Clinical Trial Site
    Bakersfield, California 93309, United States
  • Clinical Trial Site
    Beverly Hills, California 90211, United States
  • Clinical Trial Site
    Fullerton, California 92835, United States
  • Clinical Trial Site
    Irvine, California 92697, United States
  • Clinical Trial Site
    La Jolla, California 92093, United States
  • Clinical Trial Site
    Los Angeles, California 90033, United States
  • Clinical Trial Site
    Los Angeles, California 90095, United States
  • Clinical Trial Site
    Modesto, California 95356, United States
  • Clinical Trial Site
    Sacramento, California 92825, United States
  • Clinical Trial Site
    Aurora, Colorado 80045, United States
  • Clinical Trial Site
    Denver, Colorado 80246, United States
  • Clinical Trial Site
    Fort Lauderdale, Florida 33308, United States
  • Clinical Trial Site
    St. Petersburg, Florida 33711, United States
  • Clinical Trial Site
    Chicago, Illinois 60637, United States
  • Clinical Trial Site
    Oak Park, Illinois 60304, United States
  • Clinical Trial Site
    Carmel, Indiana 46290, United States
  • Clinical Trial Site
    Prairie Village, Kansas 66208, United States
  • Clinical Trial Site
    Baltimore, Maryland 21287, United States
  • Clinical Trial Site
    Boston, Massachusetts 02114, United States
  • Clinical Trial Site
    Waltham, Massachusetts 02451, United States
  • Clinical Trial Site
    Ann Arbor, Michigan 48105, United States
  • Clinical Trial Site
    Detroit, Michigan 48201, United States
  • Clinical Trial Site
    Detroit, Michigan 48202, United States
  • Clinical Trial Site
    Minneapolis, Minnesota 55455, United States
  • Clinical Trial Site
    Rochester, Minnesota 55905, United States
  • Clinical Trial Site
    St Louis, Missouri 63108, United States
  • Clinical Trial Site
    Omaha, Nebraska 68105, United States
  • Clinical Trial Site
    Palisades Park, New Jersey 07650, United States
  • NYU Langone Health
    New York, New York 10017, United States
  • Clinical Trial Site
    Rochester, New York 14642, United States
  • Clinical Trial Site
    Durham, North Carolina 27705, United States
  • Clinical Trial Site
    Winston-Salem, North Carolina 27157, United States
  • Clinical Trial Site
    Cleveland, Ohio 44106, United States
  • Clinical Trial Site
    Cleveland, Ohio 44195, United States
  • Clinical Trial Site
    Columbus, Ohio 43212, United States
  • Clinical Trial Site
    Portland, Oregon 97221, United States
  • Clinical Trial Site
    Portland, Oregon 97239, United States
  • Clinical Trial Site
    Erie, Pennsylvania 16507, United States
  • Clinical Trial Site
    Philadelphia, Pennsylvania 19107, United States
  • Clinical Trial Site
    Philadelphia, Pennsylvania 19141, United States
  • Clinical Trial Site
    Greenville, South Carolina 29605, United States
  • Clinical Trial Site
    Nashville, Tennessee 37232, United States
  • Clinical Trial Site
    Austin, Texas 78712, United States
  • Clinical Trial Site
    Bellaire, Texas 77401, United States
  • Clinical Trial Site
    Dallas, Texas 75390, United States
  • Clinical Trial Site
    Houston, Texas 77025, United States
  • Clinical Trial Site
    Katy, Texas 77494, United States
  • Clinical Trial Site
    Plano, Texas 75075, United States
  • Clinical Trial Site
    Round Rock, Texas 78681, United States
  • Clinical Trial Site
    San Antonio, Texas 78230, United States
  • Clinical Trial Site
    Madison, Wisconsin 53705, United States
  • Clinical Trial Site
    Rosario, Santa Fe Province 41076, Argentina
  • Clinical Trial Site
    Buenos Aires, 41076, Argentina
  • Clinical Trial Site
    Buenos Aires, C1015, Argentina
  • Clinical Trial Site
    Buenos Aires, C1061AAE, Argentina
  • Clinical Trial Site
    Buenos Aires, C1121, Argentina
  • Clinical Trial Site
    Sydney, New South Wales 2000, Australia
  • Clinical Trial Site
    East Melbourne, Victoria 3002, Australia
  • Clinical Trial Site
    Nedlands, Western Australia 6009, Australia
  • Clinical Trial Site
    Linz, 04020, Austria
  • Clinical Trial Site
    Leuven, VI-Brabant 3000, Belgium
  • Clinical Trial Site
    Prague, 128 08, Czechia
  • Clinical Trial Site
    Mannheim, Baden-Wurttemberg 68167, Germany
  • Clinical Trial Site
    Bonn, North Rhine-Westphalia 53127, Germany
  • Clinical Trial Site
    Düsseldorf, North Rhine-Westphalia 40225, Germany
  • Clinical Trial Site
    Münster, North Rhine-Westphalia 48145, Germany
  • Clinical Trial Site
    Münster, North Rhine-Westphalia 48149, Germany
  • Clinical Trial Site
    Kiel, 24105, Germany
  • Clinical Trial Site
    Mainz, 55131, Germany
  • Clinical Trial Site
    Thessaloniki, 54622, Greece
  • Clinical Trial Site
    Pécs, Baranya 07623, Hungary
  • Clinical Trial Site
    Debrecen, Hajdú-Bihar 04032, Hungary
  • Clinical Trial Site
    Budapest, Pest County 01085, Hungary
  • Clinical Trial Site
    Budapest, 01133, Hungary
  • Clinical Trial Site
    Ashkelon, 7830604, Israel
  • Clinical Trial Site
    Haifa, 3109601, Israel
  • Clinical Trial Site
    Haifa, 3434104, Israel
  • Clinical Trial Site
    Holon, 58101, Israel
  • Clinical Trial Site
    Jerusalem, 9013102, Israel
  • Clinical Trial Site
    Jerusalem, 9112001, Israel
  • Clinical Trial Site
    Kfar Saba, 4428164, Israel
  • Clinical Trial Site
    Poria – Neve Oved, 1528801, Israel
  • Clinical Trial Site
    Tel Aviv, 6423906, Israel
  • Clinical Trial Site
    Tel Aviv, 69710, Israel
  • Clinical Trial Site
    Perugia, Umbria 06129, Italy
  • Clinical Trial Site
    Milan, Italy
  • Clinical Trial Site
    Reggio Emilia, 42123, Italy
  • Clinical Trial Site
    Roma, 00184, Italy
  • Clinical Trial Site
    Barcelona, Catalonia 08035, Spain
  • Clinical Trial Site
    Barcelona, 08028, Spain
  • Clinical Trial Site
    Madrid, 28-046, Spain
  • Clinical Trial Site
    Madrid, 28040, Spain
  • Clinical Trial Site
    Valladolid, 47011, Spain
  • Clinical Trial Site
    London, England EC1V 2PD, United Kingdom
  • Clinical Trial Site
    London, England SE1 7EH, United Kingdom
  • Clinical Trial Site
    Maidstone, Kent ME169QQ, United Kingdom
  • Clinical Trial Site
    Middlesbrough, North Yorkshire TS4 3BW, United Kingdom
  • Clinical Trial Site
    Oxford, Oxfordshire OX3 9DU, United Kingdom

Showing the first 100 of 107 sites across 13 countries. Choose a country and city above to see the rest.

08

References and documents

Related links

Individual participant data

Plan to share: Undecided

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06431373
Lead sponsor
Priovant Therapeutics, Inc.
Responsible party
Sponsor
First posted
May 28, 2024
Start date
Sep 11, 2024
Primary completion
Sep 11, 2026 (estimated)
Completion
Feb 1, 2028 (estimated)
Last update
Jan 12, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion