Summary

Eligibility
for people ages 18-74 (full criteria)
Location
at UCLA
Dates
study started
completion around

Description

Summary

This study will evaluate the clinical safety and efficacy of oral brepocitinib in participants with active intermediate, posterior, or pan non-infectious uveitis (NIU).

Official Title

A Phase 2 Randomized, Double-Masked, Dose-Ranging Study to Investigate the Safety and Efficacy of Oral Brepocitinib in Adults With Active Non-Infectious Intermediate-, Posterior-, and Panuveitis

Keywords

Non-infectious Intermediate Uveitis, Non-infectious Posterior Uveitis, Non-infectious Pan Uveitis, Brepocitinib, PF-06700841, uveitis, NIU, Posterior Uveitis, Intermediate Uveitis, Pars Planitis, Panuveitis

Eligibility

You can join if…

Open to people ages 18-74

  1. Adult subjects (18-74 years old)
  2. Diagnosis of non-infectious uveitis (intermediate uveitis, posterior uveitis, or panuveitis).
  3. Active uveitic disease as defined by the presence of at least 1 of the following parameters in at least 1 eye, as determined by the investigator:
    1. Active, inflammatory chorioretinal and/or retinal vascular lesion; OR
    2. ≥2+ vitreous haze grade (NEI/SUN criteria).
  4. Receiving up to one non-corticosteroid, non-biologic, immunomodulatory therapy
  5. Weight > 40 kg with a body mass index < 40 kg/m2.

You CAN'T join if...

  1. Has isolated anterior uveitis.
  2. Has confirmed or suspected current diagnosis of infectious uveitis
  3. History of:
  4. At risk of thrombosis and cardiovascular disease
  5. Have a high risk for herpes zoster reactivation
  6. Have active or recent infections

Other protocol defined Inclusion/Exclusion criteria may apply

Locations

  • Clinical Trial Site
    Los Angeles California 90095 United States
  • Clinical Trial Site
    Pasadena California 91107 United States
  • Clinical Trial Site
    Palo Alto California 94303 United States

Details

Status
in progress, not accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Priovant Therapeutics, Inc.
Links
Study Website
ID
NCT05523765
Phase
Phase 2 Uveitis Research Study
Study Type
Interventional
Participants
About 26 people participating
Last Updated