Efficacy and Safety of Baricitinib in Neuromyelitis Optica Spectrum Disorders

Recruiting Phase 1 Phase 2 Interventional Study
NMO Spectrum Disorder
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 85
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Basic Science
Participants needed
12 (estimated)
Sponsor
Tianjin Medical University General Hospital · Other
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About This Trial
Neuromyelitis Optica Spectrum Disorders (NMOSD) is associated with a pathological humoral immune response against the aquaporin-4(AQP-4) water channel. Baricitinib is an oral Janus kinase (JAK)1/JAK2 inhibitor that blocks the upregulated JAK-STAT pathway in patients with neuroimmune disorders, which is important in bone marrow regulation of B cell proliferation and differentiation. Baricitinib may…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Male or female patients ≥ 18 years old; 2. Diagnosis of NMO or NMO spectrum disorder according to the 2015 International Panel for Neuromyelitis Optica Diagnosis criteria; 3. Clinical evidence of either at least one attack requiring rescue therapy (intravenous corticosteroids…
Contacts

Qiang Liu, M.D.,Ph.D.

+86 15022439149

qliu@tmu.edu.cn

CONTACT