Myasthenia Gravis Treatments Chart

Medicine Class Antibody Criteria Delivery Frequency
Acetylcholinesterase inhibitor The original first-line therapy for MG — increases the amount of acetylcholine available at the neuromuscular junction. Fast acting, but treats symptoms rather than the underlying immune attack.
Mestinon pyridostigmine bromide AChE inhibitor Not antibody-specific Oral tablet, extended-release tablet, or liquid Multiple times per day (fast-acting); 1–2x/day for extended-release

Mestinon

Generic name
pyridostigmine bromide
Antibody criteria
Not antibody-specific
Delivery method
Oral tablet, extended-release tablet, or liquid
Frequency
Multiple times per day (fast-acting); 1–2x/day for extended-release
Dosage
Individualized and titrated to effect; commonly 60 mg tablets every 3–8 hours, or 180 mg extended-release once or twice daily, at least 6 hours apart.
Common side effects
Stomach cramps, diarrhea, nausea, increased saliva and sweating.
Serious side effects
Cholinergic crisis from too much medicine can cause worsening weakness and breathing trouble — it can look like a myasthenic crisis, so any new weakness needs prompt medical attention.
FDA status
FDA-approved for MG
Manufacturer
Bausch Health (brand); generic pyridostigmine widely available
Assistance program
Ask your pharmacist about generic discount programs; no dedicated manufacturer program
Corticosteroids & non-steroidal immunosuppressants Broadly dampen the immune system to reduce the antibodies attacking the neuromuscular junction. Usually the next step after acetylcholinesterase inhibitors.
Prednisone prednisone Corticosteroid / immunosuppressant Not antibody-specific Oral tablet Daily, or every other day once symptoms are controlled

Prednisone

Generic name
prednisone
Antibody criteria
Not antibody-specific
Delivery method
Oral tablet
Frequency
Daily, or every other day once symptoms are controlled
Dosage
Individualized — usually started low and increased gradually until symptoms improve, then tapered to the lowest effective dose.
Common side effects
Weight gain, increased appetite, mood changes, trouble sleeping, elevated blood sugar.
Serious side effects
High blood pressure, stomach ulcers, increased infection risk, bone thinning (osteoporosis) with long-term use.
FDA status
FDA-approved (generic corticosteroid)
Manufacturer
Generic; multiple manufacturers
Assistance program
Low-cost generic; dedicated assistance programs generally not needed
CellCept mycophenolate mofetil Corticosteroid / immunosuppressant Not antibody-specific · Off-label use Oral tablet, capsule, or liquid Twice daily

CellCept

Generic name
mycophenolate mofetil
Antibody criteria
Not antibody-specific · Off-label use
Delivery method
Oral tablet, capsule, or liquid
Frequency
Twice daily
Dosage
Individualized; may take 6–12 months for full benefit.
Common side effects
Diarrhea, nausea, low blood cell counts, increased infection risk.
Serious side effects
BOXED WARNING Boxed warning: increased risk of pregnancy loss and birth defects.
FDA status
Off-label for MG (FDA-approved for transplant rejection)
Manufacturer
Genentech (brand); generic mycophenolate mofetil widely available
Assistance program
Genentech patient resource center (gene.com/patients)
Cyclosporine cyclosporine Corticosteroid / immunosuppressant Not antibody-specific · Off-label use Oral tablet or capsule Twice daily

Cyclosporine

Generic name
cyclosporine
Antibody criteria
Not antibody-specific · Off-label use
Delivery method
Oral tablet or capsule
Frequency
Twice daily
Dosage
Weight-based, individualized, and adjusted using blood level monitoring.
Common side effects
Tremor, gum overgrowth, excess hair growth, headache.
Serious side effects
Kidney damage, high blood pressure, increased infection risk — requires regular blood pressure and kidney-function monitoring.
FDA status
Off-label for MG
Manufacturer
Generic; brand names Neoral® / Sandimmune® (Novartis)
Assistance program
Ask your pharmacist about generic discount programs
Imuran azathioprine Corticosteroid / immunosuppressant Not antibody-specific · Off-label use Oral tablet Once or twice daily

Imuran

Generic name
azathioprine
Antibody criteria
Not antibody-specific · Off-label use
Delivery method
Oral tablet
Frequency
Once or twice daily
Dosage
Individualized, weight-based; benefit can take 4–12 months to appear.
Common side effects
Nausea, flu-like symptoms, low white blood cell counts.
Serious side effects
BOXED WARNING Boxed warning: increased risk of malignancy with long-term use.
FDA status
Off-label for MG
Manufacturer
Sebela Pharmaceuticals (brand); generic azathioprine widely available
Assistance program
Ask your pharmacist about generic discount programs
B-cell directed therapies Target the B-cells that manufacture the antibodies responsible for MG symptoms.
Rituximab rituximab (brand Rituxan®; biosimilars available) B-cell directed MuSK+ · AChR+ · Off-label use IV infusion, in cycles Protocols vary — e.g. weekly ×4, or 2 doses 2 weeks apart — repeated roughly every 6–12 months based on response

Rituximab

Generic name
rituximab (brand Rituxan®; biosimilars available)
Antibody criteria
MuSK+ · AChR+ · Off-label use
Delivery method
IV infusion, in cycles
Frequency
Protocols vary — e.g. weekly ×4, or 2 doses 2 weeks apart — repeated roughly every 6–12 months based on response
Dosage
Protocol-dependent, e.g. 375 mg/m² weekly ×4 weeks, or 1,000 mg on days 1 and 15.
Common side effects
Infusion reactions, fatigue, body aches.
Serious side effects
BOXED WARNING Boxed warning (on Rituxan label): infusion reactions, severe skin reactions, hepatitis B reactivation, PML.
FDA status
Off-label for MG (FDA-approved for lymphoma, rheumatoid arthritis, other conditions)
Manufacturer
Genentech/Biogen (brand Rituxan®); biosimilars available
Assistance program
Genentech BioOncology Co-pay Program (for brand); biosimilar-specific programs vary
UPLIZNA inebilizumab-cdon B-cell directed AChR+ · MuSK+ IV infusion 2 initial infusions 2 weeks apart, then 1 infusion every 6 months

UPLIZNA

Generic name
inebilizumab-cdon
Antibody criteria
AChR+ · MuSK+
Delivery method
IV infusion
Frequency
2 initial infusions 2 weeks apart, then 1 infusion every 6 months
Dosage
300 mg per infusion.
Common side effects
Infusion reactions, low blood cell counts, respiratory and urinary tract infections.
Serious side effects
Infusion reactions including anaphylaxis; increased infection risk; potential hepatitis B reactivation.
FDA status
FDA-approved for gMG (December 2025)
Manufacturer
Amgen
Assistance program
Amgen By Your Side
Neonatal Fc receptor (FcRn) blockers Block the receptor that normally protects IgG antibodies from being broken down — clearing out the harmful antibodies faster.
IMAAVY nipocalimab-aahu FcRn blocker AChR+ · MuSK+ IV infusion (first dose ~30 min, then ~15 min) Every 2 weeks, after the first infusion

IMAAVY

Generic name
nipocalimab-aahu
Antibody criteria
AChR+ · MuSK+
Delivery method
IV infusion (first dose ~30 min, then ~15 min)
Frequency
Every 2 weeks, after the first infusion
Dosage
Weight-based, supplied as 300 mg or 1,200 mg single-dose vials.
Common side effects
Common cold-type infections, headache, infusion-related reactions.
Serious side effects
Increased infection risk; vaccines may be less effective during treatment.
FDA status
FDA-approved for gMG, ages 12+ (April 2025)
Manufacturer
Johnson & Johnson
Assistance program
IMAAVY withMe
Rystiggo rozanolixizumab-noli FcRn blocker AChR+ · MuSK+ Subcutaneous infusion, given by a healthcare professional Once weekly for 6 weeks per cycle; cycles repeated based on symptoms

Rystiggo

Generic name
rozanolixizumab-noli
Antibody criteria
AChR+ · MuSK+
Delivery method
Subcutaneous infusion, given by a healthcare professional
Frequency
Once weekly for 6 weeks per cycle; cycles repeated based on symptoms
Dosage
Weight-based, 280–840 mg per weekly dose.
Common side effects
Headache, infections, diarrhea, fever, nausea, hypersensitivity reactions.
Serious side effects
Increased infection risk, hypersensitivity reactions (including angioedema), drug-induced aseptic meningitis.
FDA status
FDA-approved for gMG (2023) — only therapy approved for both AChR+ and MuSK+ gMG
Manufacturer
UCB
Assistance program
ONWARD (UCB) + Rystiggo Patient Savings Program
Vyvgart efgartigimod alfa-fcab FcRn blocker AChR+ · MuSK+ · LRP4+ / seronegative IV infusion (~1 hour) 4 weekly infusions per cycle; cycles repeated based on symptoms

Vyvgart

Generic name
efgartigimod alfa-fcab
Antibody criteria
AChR+ · MuSK+ · LRP4+ / seronegative
Delivery method
IV infusion (~1 hour)
Frequency
4 weekly infusions per cycle; cycles repeated based on symptoms
Dosage
10 mg/kg per infusion (weight-based).
Common side effects
Respiratory and urinary tract infections, headache.
Serious side effects
Increased infection risk; hypersensitivity reactions including anaphylaxis.
FDA status
FDA-approved for gMG — all serotypes: AChR+, MuSK+, LRP4+, and seronegative
Manufacturer
argenx
Assistance program
My VYVGART Path
Vyvgart Hytrulo efgartigimod alfa and hyaluronidase-qvfc FcRn blocker AChR+ · MuSK+ · LRP4+ / seronegative Subcutaneous injection (20–90 seconds); can be self-administered at home after training 4 weekly injections per cycle; cycles repeated based on symptoms

Vyvgart Hytrulo

Generic name
efgartigimod alfa and hyaluronidase-qvfc
Antibody criteria
AChR+ · MuSK+ · LRP4+ / seronegative
Delivery method
Subcutaneous injection (20–90 seconds); can be self-administered at home after training
Frequency
4 weekly injections per cycle; cycles repeated based on symptoms
Dosage
Fixed-dose prefilled syringe or vial (not weight-based).
Common side effects
Respiratory and urinary tract infections, injection site reactions, headache.
Serious side effects
Increased infection risk; hypersensitivity reactions.
FDA status
FDA-approved for gMG — all serotypes: AChR+, MuSK+, LRP4+, and seronegative
Manufacturer
argenx
Assistance program
My VYVGART Path
Complement (C5) inhibitors Block the complement cascade that damages the neuromuscular junction after antibodies attach. All carry a boxed warning for serious meningococcal infection and require REMS enrollment.
Soliris eculizumab C5 inhibitor AChR+ IV infusion (~35 minutes) Weekly for the first 5 doses, then every 2 weeks

Soliris

Generic name
eculizumab
Antibody criteria
AChR+
Delivery method
IV infusion (~35 minutes)
Frequency
Weekly for the first 5 doses, then every 2 weeks
Dosage
900 mg weekly ×4, 1,200 mg at week 5, then 1,200 mg every 2 weeks.
Common side effects
Headache, upper respiratory infection, nausea, musculoskeletal pain.
Serious side effects
BOXED WARNING Boxed warning: life-threatening meningococcal infections. Available only through the Soliris REMS program.
FDA status
FDA-approved for gMG (2017), AChR+
Manufacturer
Alexion, AstraZeneca Rare Disease
Assistance program
Alexion OneSource™
Ultomiris ravulizumab-cwvz C5 inhibitor AChR+ IV infusion (30 min – 1 hour, weight-based) Loading dose, a second dose 2 weeks later, then every 8 weeks

Ultomiris

Generic name
ravulizumab-cwvz
Antibody criteria
AChR+
Delivery method
IV infusion (30 min – 1 hour, weight-based)
Frequency
Loading dose, a second dose 2 weeks later, then every 8 weeks
Dosage
Weight-based: loading 2,400–3,000 mg, maintenance 3,000–3,600 mg.
Common side effects
Diarrhea, upper respiratory infection, headache.
Serious side effects
BOXED WARNING Boxed warning: life-threatening meningococcal infections. Available only through the Ultomiris REMS program.
FDA status
FDA-approved for gMG (2022), AChR+
Manufacturer
Alexion, AstraZeneca Rare Disease
Assistance program
Alexion OneSource™
Zilbrysq zilucoplan C5 inhibitor AChR+ Subcutaneous injection, self-administered Once daily

Zilbrysq

Generic name
zilucoplan
Antibody criteria
AChR+
Delivery method
Subcutaneous injection, self-administered
Frequency
Once daily
Dosage
Weight-based; supplied as 16.6 mg, 23 mg, or 32.4 mg prefilled syringes.
Common side effects
Injection site reactions, diarrhea, upper respiratory infection.
Serious side effects
BOXED WARNING Boxed warning: life-threatening meningococcal infections. Available only through the Zilbrysq REMS program.
FDA status
FDA-approved for gMG (2023), AChR+
Manufacturer
UCB
Assistance program
ONWARD (UCB)

Not daily or cyclical drug therapies, but part of the MG treatment landscape — used for emergencies, as a bridge, or as a one-time procedure.

IVIg (intravenous immunoglobulin)

Infusion · Emergency or maintenance

Donated, pooled antibodies given by IV. Used as a short-term emergency treatment (myasthenic crisis, before surgery) over 2–5 days, or as maintenance every 3–6 weeks. Common side effects include headache, chills, and flu-like symptoms; rare serious effects include kidney problems and blood clots.

Hizentra (subcutaneous immunoglobulin)

CSL Behring · Not yet FDA-approved for MG

A less-invasive way to receive immunoglobulins, given under the skin at up to 8 sites over 1–2 hours, often at home. Approved for other neurologic and immune conditions; use in MG is still investigational.

Therapeutic plasma exchange

Plasmapheresis · Emergency use

Filters the blood to remove antibody-containing plasma, replacing it with clean fluid, via a vein or port. Used short-term for emergencies or before surgery; repeated treatments are often needed since the body keeps producing antibodies.

Thymectomy

Surgery · One-time procedure

Surgical removal of the thymus gland. Strongly recommended if a thymoma is present, and often considered earlier in AChR+ generalized MG to improve long-term symptoms and reduce reliance on corticosteroids.