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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported