Set Your Location to See Relevant Information

Setting your location helps us to show you nearby providers and locations based on your healthcare needs.

GN41791

GN41791

Objective

A Phase III Multicenter, Randomized, Double-Blind, Double-Dummy, Parallel-Group Study to Evaluate the Efficacy and Safety of Fenebrutinib Compared with Ocrelizumab in Adult Patients with Primary Progressive Multiple Sclerosis

The MS Center at EvergreenHealth is conducting a Phase III, randomized, double-blind, double-dummy,
parallel-group study to evaluate the efficacy and safety of fenebrutinib on disability progression in adult patients with primary progressive multiple sclerosis (PPMS).

In this study, patients will receive fenebrutinib (or placebo) and ocrelizumab (or placebo).

Who may be eligible to participate?

Patients 18 to 65 years of age with PPMS may be eligible to participate. Other inclusion and exclusion criteria apply.

What does participation involve?

This study will consist of the following phases:

  • screening (for up to four weeks)
  • double-blind treatment (DBT) phase
  • DBT safety follow-up (DBT-SFU)
  • optional open-label extension (OLE)
  • OLE safety follow-up (OLE-SFU) phase

All eligible patients will be randomized 1:1 to either daily fenebrutinib (or placebo) or ocrelizumab (or placebo).

Investigator

Theodore Brown, MD, MPH, EvergreenHealth MS Center

Clinical Trial Categories

  • Multiple Sclerosis
Contact
EvergreenHealth Research Services at 425-899-5385
or EvergreenResearch@evergreenhealth.com