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A Study of Orelabrutinib in Patients With Secondary Progressive Multiple Sclerosis

RecruitingPhase 3

A Phase 3, Randomized, Double-blind, Efficacy and Safety Study Comparing Orelabrutinib to Placebo in Patients With Non-active Secondary Progressive Multiple Sclerosis

Who can join

Ages 18 to 60 · All sexes

Full eligibility criteria
Inclusion Criteria:

1. 18 to 60 years of age, inclusive, at the time of signing the informed consent.
2. Participant must have a previous diagnosis of RRMS in accordance with 2024 McDonald criteria
3. Participant must have a current diagnosis of SPMS in accordance with the clinical course criteria revised in 2013
4. Participant must have documented evidence of disability progression independent of clinical relapse observed during the 24 months before screening. A written summary of the clinical evidence of disability progression must be discussed and aligned between the Investigator and the Sponsor's dedicated qualified person(s).
5. Absence of clinical relapses for at least 24 months.

Exclusion Criteria:

1. The patient has been diagnosed with primary progressive MS (PPMS) according to 2024 McDonald diagnostic criteria
2. Immunologic disorder other than MS or any other conditions requiring corticosteroid therapy.
3. History or current diagnosis of other neurological disorders that may mimic MS
4. History or current diagnosis of progressive multifocal leukoencephalopathy
5. Active, clinically significant viral, bacterial, or fungal infection
6. History of any other significant active medical condition
7. History of suicidal behavior within 6 months prior to Screening
8. Any prior history of malignancy
9. Patients on anticoagulation, or antiplatelet therapy
10. Patients took strong/moderate CYP3A inhibitors or strong/moderate CYP3A inducers within 14 days
11. Clinically significant laboratory abnormalities at Screening.
12. Vaccination with live or live-attenuated virus vaccine within 1 month prior to Screening
13. History of alcohol abuse or alcohol use disorder or other drug abuse within 12 months prior to screening.

About the study

Orelabrutinib is a CNS-penetrable BTK inhibitor. This is a phase 3, randomized, double-blind, parallel-group, multicenter study to evaluate the efficacy and safety of orelabrutinib compared with placebo in patients with non-active Secondary Progress MS. Patients will be treated for approximately 24 to 60 months, with a minimum treatment duration of 12 months. The study will enroll approximately 990 subjects in a 2:1 randomization (orelabrutinib: placebo), globally.

What is being tested

Sponsor: Zenas BioPharma (USA), LLC · Participants: 990 · Started: Mar 23, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07299019

Locations in the U.S.

ArizonaArizona Neuroscience Research, LLC, Phoenix
Perseverance Research Center, LLC (PRC), Scottsdale
CaliforniaFullerton Neurology and Headache Center, Fullerton
Harbor-UCLA Medical Center - The Lundquist Institute (Los Angeles Biomedical Research Institute (LA BioMed)), Torrance
Regina Berkovich MD, PhD Inc, West Hollywood
FloridaSFM Clinical Research, LLC, Boca Raton
Nova Clinical Research, LLC, Bradenton
MS and Neuromuscular Center of Excellence, Clearwater
Neurology Associates, Maitland
Aqualane Clinical Research, Naples
University of South Florida Department of Neurology - MS Division, Tampa
IndianaJosephson Wallack Munshower Neurology, Pc Suite 225, Indianapolis
KansasKC Research Center, PA Neurology Research Dept, Roeland Park
MichiganProfound Research LLC at Oakland Neurology Center, Rochester Hills
MissouriWashington University School of Medicine, St Louis
OhioThe Boster Center for Multiple Sclerosis, Columbus
The Ohio State University Wexner Medical Center (OSUWMC), Columbus
OklahomaOMRF Multiple Sclerosis Center of Excellence, Oklahoma City
South CarolinaPremier Neurology, Greenville
TennesseeNeurology Clinic, P.C., Cordova
TexasLone Star Neurology, San Antonio
Texas Institute for Neurological Disorders - Sherman, Sherman

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.