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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

  • Sex: Any
  • Age: Adult (18 - 64), Older Adult (65+)
  • Accepting Healthy People: No
  • Type: Interventional / Therapeutic
  • Trial Phase: Phase III
  • Conditions Being Studied: Uveitis

Study Purpose

The purpose of this clinical research study is to learn more about the use of an investigational medicine, called brepocitinib, for the treatment of active non-infectious intermediate-, posterior- or pan-uveitis, or NIU (non-infectious uveitis) for short. Brepocitinib (“study drug”) works by decreasing inflammation. This study is being done to determine how safe and effective brepocitinib is and if it works to help decrease the inflammation associated with NIU and will monitor the long-term safety of brepocitinib when taken for a period up to 96 weeks.

Who Can Participate

Age: 18-75 years old

Principal Investigator
Shree Kurup MD
Department/Division
Ophthalmology (Retina)

Locations

UH Cleveland Medical Center
11100 Euclid Avenue
Cleveland OH, 44106

  • UH IRB: SITE00002288
  • StudyID: 2024-01524
  • ClinicalTrials.gov: NCT06431373
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