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Search / Trial NCT06431373

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

Launched by PRIOVANT THERAPEUTICS, INC. · May 22, 2024

Trial Information

Current as of July 22, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying a new medication called brepocitinib to see how safe and effective it is for adults with active, non-infectious uveitis, a condition that causes inflammation in the eyes. Specifically, the trial is looking at patients with intermediate, posterior, or pan uveitis, which means the inflammation affects different parts of the eye but is not caused by an infection. Researchers hope to determine if this treatment can help reduce symptoms and improve eye health.

To participate in the study, you must be an adult between 18 and 75 years old, diagnosed with non-infectious uveitis in at least one eye, and have a body weight over 40 kg. However, you cannot join if you have certain health conditions, like infectious uveitis, active cancer, or recent serious infections. If you qualify and decide to participate, you will receive the study medication and be closely monitored for any side effects or improvements in your condition. This trial is currently recruiting participants, and it offers a chance to help advance treatments for uveitis while receiving care from experienced medical professionals.

Gender

ALL

Eligibility criteria

  • 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 body mass index ≤ 40 kg/m2
  • Exclusion Criteria:
  • Has confirmed or suspected current diagnosis of infectious uveitis History of or have:
  • 1. Lymphoproliferative disorder
  • 2. active malignancy
  • 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 orand cerebrovascularardiovascular ischemic event disease within the last 12 months
  • 5. a high risk for herpes zoster reactivation
  • 6. active or recent infections

About Priovant Therapeutics, Inc.

Priovant Therapeutics, Inc. is a biopharmaceutical company focused on advancing innovative therapies for patients with autoimmune and inflammatory diseases. Leveraging a robust pipeline and a commitment to scientific excellence, Priovant aims to address significant unmet medical needs through the development of novel treatments that enhance patient outcomes. The company's strategic approach combines cutting-edge research with a dedication to collaboration, ensuring the delivery of safe and effective therapies. With a strong emphasis on clinical development and patient-centric solutions, Priovant Therapeutics is poised to make a meaningful impact in the field of immunology.

Locations

Dallas, Texas, United States

New York, New York, United States

Philadelphia, Pennsylvania, United States

Cleveland, Ohio, United States

Los Angeles, California, United States

Durham, North Carolina, United States

Aurora, Colorado, United States

Boston, Massachusetts, United States

Rochester, Minnesota, United States

Detroit, Michigan, United States

Portland, Oregon, United States

Houston, Texas, United States

Fort Lauderdale, Florida, United States

Nashville, Tennessee, United States

Austin, Texas, United States

Round Rock, Texas, United States

La Jolla, California, United States

Minneapolis, Minnesota, United States

Madison, Wisconsin, United States

Waltham, Massachusetts, United States

Palisades Park, New Jersey, United States

Bellaire, Texas, United States

Plano, Texas, United States

Beverly Hills, California, United States

Omaha, Nebraska, United States

Katy, Texas, United States

Bakersfield, California, United States

Philadelphia, Pennsylvania, United States

Phoenix, Arizona, United States

Fullerton, California, United States

Sacramento, California, United States

Carmel, Indiana, United States

Ann Arbor, Michigan, United States

Erie, Pennsylvania, United States

Irvine, California, United States

Modesto, California, United States

Saint Petersburg, Florida, United States

Saint Louis, Missouri, United States

Portland, Oregon, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported