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NMOSD & MOGAD Treatment

Treatment options for AQP4-IgG NMOSD and MOGAD in one view. The Disease & approval column shows what each agent is FDA-approved or used for — note all 4 FDA-approved drugs are AQP4-NMOSD only; MOGAD is treated off-label (no FDA-approved MOGAD therapy exists as of 2026). Verify dosing/screening against current prescribing information.

DrugDisease & approvalMechanismDose / routeKey side effectsClinical tips
FDA-approved maintenance — adult AQP4-IgG NMOSD
Eculizumab (Soliris)NMOSD (AQP4+) — FDA 2019Terminal complement C5 inhibitor900 mg IV weekly ×4, then 1200 mg q2 wkMeningococcal infection (boxed warning), infusion reactions, headache, URTIMeningococcal vaccine ≥2 wk before (or antibiotic prophylaxis); no role in AQP4-negative or MOGAD
Ravulizumab (Ultomiris)NMOSD (AQP4+) — FDA 2024Long-acting C5 inhibitorWeight-based IV load, then q8 wkMeningococcal infection (boxed warning), infections, headacheMuch longer dosing interval than eculizumab; meningococcal vaccination required
Inebilizumab (Uplizna)NMOSD (AQP4+) — FDA 2020Anti-CD19 B-cell depletion300 mg IV day 1 & 15, then q6 moInfusion reactions, infections, hypogammaglobulinemia, lymphopenia, HBV reactivationScreen HBV/TB, quantitative Ig, vaccines; broader B-cell depletion than anti-CD20
Satralizumab (Enspryng)NMOSD (AQP4+) — FDA 2020IL-6 receptor antagonist120 mg SC wk 0/2/4, then q4 wkInfections, injection reactions, ↑ LFTs, ↓ neutrophilsSC self-injection; monitor LFTs/neutrophils; IL-6 blockade can blunt CRP/fever (mask infection)
Off-label maintenance — NMOSD ± MOGAD
RituximabNMOSD off-label (1st-line) · MOGAD off-label (less reliable)Anti-CD20 B-cell depletion1 g IV ×2 (2 wk apart) or 375 mg/m²; redose q6 mo or by B-cell returnInfusion reactions, infections, hypogammaglobulinemia, HBV reactivation, rare PMLTime redosing by CD19/CD27 memory B-cell reconstitution; HBV screen; widely used in both diseases
TocilizumabBoth (off-label; refractory)IL-6 receptor antagonist (IV/SC)8 mg/kg IV q4 wkInfections, ↑ LFTs, ↓ neutrophils/platelets, GI perforation, ↑ lipidsFor disease refractory to B-cell depletion; monitor LFTs/CBC/lipids
AzathioprineBoth (off-label; maintenance)Purine antimetabolite2–3 mg/kg/day POMyelosuppression, hepatotoxicity, ↑ malignancy, GICheck TPMT / NUDT15 + CBC/LFT; slow onset (~3–6 mo) → bridge with steroids
Mycophenolate mofetilBoth (off-label; maintenance)Inhibits IMPDH (purine synthesis)1–1.5 g PO BIDGI upset, leukopenia, infection, teratogenicBridge with steroids at start; contraception required; monitor CBC
IVIGMOGAD maintenance (off-label, esp. pediatric); acute rescueImmunomodulation (multiple)1–2 g/kg q4 wk (maintenance varies)Headache, aseptic meningitis, thrombosis, renal, anaphylaxis (IgA deficiency)Preferred maintenance in MOGAD, esp. children; acute use mainly MOGAD rescue (not standard acute NMOSD); check IgA
Acute attack — both diseases
IV methylprednisoloneBoth (acute, 1st-line)High-dose corticosteroid1 g IV daily ×3–5 daysHyperglycemia, insomnia, mood change, infectionFirst-line for acute attacks; often followed by an oral taper (esp. MOGAD, which is steroid-dependent)
Plasma exchange (PLEX)Both (acute; steroid-refractory)Removes circulating autoantibodies5–7 exchanges every other dayLine complications, hypocalcemia, coagulopathy, hypotensionEarly PLEX improves recovery in severe NMOSD attacks — consider first-line for severe/refractory attacks
⚠ Avoid MS disease-modifying therapies in AQP4-NMOSD — interferon-β, natalizumab, fingolimod / S1P modulators, and alemtuzumab can worsen AQP4-NMOSD; glatiramer is ineffective. Confirm AQP4/MOG serostatus before any “MS” DMT. MS DMTs are also generally ineffective in MOGAD. When to start maintenance: AQP4+ NMOSD — after the first attack; MOGAD — usually after a relapse or severe residual deficit (many monophasic cases need none).

Neuro-Pharmacology — NeurologyResident.Net by Ahmed Koriesh