Skip to main content

Pegcetacoplan

Pronunciation: peg-SET-a-KOE-plan
Generic name: pegcetacoplan
Brand name: Empaveli
Dosage form: injection, for subcutaneous use via an infusion pump or Empaveli injector (1080 mg/20 mL)
Drug class: Selective immunosuppressants

Medically reviewed by Carmen Pope, BPharm. Last updated on July 31, 2025.

What is pegcetacoplan?

Pegcetacoplan (brand name Empaveli) is a twice-weekly, injectable medicine that is used to treat adults with paroxysmal nocturnal hemoglobinuria (PNH) or to reduce proteinuria in adults and children 12 years and older with C3 glomerulopathy (C3G) or primary immune-complex membranoproliferative glomerulonephritis (IC-MPGN). It is given by subcutaneous infusion using an infusion pump or the on-body Empaveli injector. 

Pegcetacoplan works by targeting the immune system, and its mechanism of action (MOA) in PNH is to block a specific protein (C3) involved in breaking down red blood cells. This helps prevent intravascular hemolysis (IVH, the destruction of red blood cells in the circulation) and extravascular hemolysis (EVH, the breakdown of red blood cells in the spleen, bone marrow, or liver by macrophages). Pegcetacoplan is the only treatment that targets C3 and may prevent both forms of red blood cell destruction (IVH and EVH). It works higher in the complement system than other treatments used for PNH.

In C3G and primary IC-MPGN, excessive complement activity causes harmful C3 fragment deposits in kidney filters, leading to damage. Pegcetacoplan targets C3 and C3b proteins, interrupting the complement pathway to prevent toxic accumulation and reduce renal inflammation and injury.

Because of the risk of infections, pegcetacoplan is only available under the brand name Empaveli and through a restricted program called the Empaveli REMS. Your healthcare provider must be a member of this program to be able to prescribe pegcetacoplan and provide you with the necessary information and a Patient Safety Card. Only pharmacies certified for the Empaveli REMS program can dispense Empaveli.

Pegcetacoplan gained FDA approval on May 14, 2021, under the brand, Empaveli, for PNH. Approval was extended on July 28, 2025, to include C3G and IC-MPGN. There is no Empaveli generic available. Intravitreal pegcetacoplan gained FDA approval on February 17, 2023, under the brand name Syfovre.

Apellis Pharmaceuticals makes pegcetacoplan for PNH, C3G and IC-MPGN.

Pegcetacoplan side effects

The most common side effects of pegcetacoplan for PNH include:

The most common side effects of pegcetacoplan for C3G or primary IC-MPGN are:

Serious side effects and warnings

Pegcetacoplan can cause serious side effects, such as serious infections by encapsulated bacteria.

Pegcetacoplan can lower the ability of your immune system to fight infections and increase your risk of developing serious and life-threatening infections, including meningitis caused by encapsulated bacteria such as Streptococcus pneumoniae; Neisseria meningitidis, types A, C, W, Y, and B; and Haemophilus influenzae type B. You must be vaccinated against these bacteria at least 2 weeks before your first dose if you have not already had these vaccines. If your healthcare provider decides that urgent treatment with pegcetacoplan is needed, you should receive the required vaccinations as soon as possible. Meningococcal infections may quickly become life-threatening and cause death if not recognized and treated early. Call your healthcare provider or get emergency medical care right away if you get any of these signs and symptoms of a serious infection once you have started taking pegcetacoplan:

May cause infusion-related reactions or allergic reactions including anaphylaxis which may be life-threatening. Stop your infusion and seek immediate medical attention if you develop any of the following: difficulty breathing, including shortness of breath and wheezing; swollen face, tongue or throat; feeling faint; rapid heart rate; skin reactions, including hives and itching; nausea or vomiting; confusion and anxiety; dizziness or fainting. If any of these symptoms happen during an infusion, stop your infusion and tell your healthcare provider or get emergency medical care right away.

After stopping pegcetacoplan, patients with PNH will be closely monitored by their healthcare provider for at least 8 weeks for dangerous red blood cell breakdown (hemolysis). Warning signs include elevated LDH levels, fatigue, dark urine, stomach pain, breathing problems, blood clots, swallowing difficulties, or erectile dysfunction. If hemolysis occurs, consider restarting pegcetacoplan.

May interfere with laboratory tests, such as those that use silica reagents in coagulation panels (may cause an artificially prolonged activated partial thromboplastin time [aPTT]).

It is not known if pegcetacoplan is safe and effective in children.

Tell your healthcare provider about any side effect that bothers you or that does not go away. These are not all of the possible side effects. For more information, ask your healthcare provider or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088 or contact Apellis Pharmaceuticals, Inc. at 1-833-866-3346.

Before taking this medicine

Do not take pegcetacoplan if you:

Before you take pegcetacoplan, tell your healthcare provider about all of your medical conditions, including if you:

Pregnancy and breastfeeding

Pegcetacoplan may harm your unborn baby. Females who can become pregnant should have a pregnancy test before starting treatment and use an effective method of birth control (contraception) during treatment, and for 40 days after the final dose.

Breastfeeding

It is not known if pegcetacoplan passes into breast milk. You should not breastfeed during treatment, and for 40 days after the final dose.

How should I take pegcetacoplan?

Pegcetacoplan is given subcutaneously (this means under the skin) using an infusion pump or the Empaveli injector. Use this medicine exactly as your healthcare provider tells you. Do not infuse more or less than your healthcare provider tells you to.

Your healthcare provider will give you an Empaveli Patient Safety Card about the risk of serious infections. Carry it with you at all times during treatment and for 2 months after your last dose. Your risk of serious infections may continue for several weeks after your last dose. It is important to show this card to any healthcare provider who treats you. This will help them diagnose and treat you quickly.

Dosing information

Dose of Pegcetacoplan for PNH for adults:

Dose of Pegcetacoplan for C3G or IC-MPGN 

Body weight First dose (infusion volume) Second dose (infusion volume) Maintenance dose (infusion volume)
50 kg or higher 1080 mg (20 mL) 1080 mg (20 mL) 1080 mg (20 mL) twice weekly
35 kg to less than 50 kg 648 mg (12 mL) 810 mg (15 mL) 810 mg (15 mL) twice weekly
Less than 35 kg 540 mg (10 mL) 540 mg (10 mL) 648 mg (12 mL) twice weekly

Administration of pegcetacoplan via an infusion pump

It should be administered into a clear area of skin on your stomach (avoid around the belly button), or the top of your thighs, hips, or upper arms.

Administration of pegcetacoplan via the Empaveli injector

The Empaveli injector is a compact, single-use device that is attached to your body and delivers your dose of pegcetacoplan subcutaneously (under the skin) of your abdomen, allowing you greater mobility while the infusion is in process.

What happens if I miss a dose?

If you miss a dose, take the missed dose as soon as possible. Take your next dose at your regularly scheduled time.

Do not stop taking pegcetacoplan without your doctor's advice. After stopping it, your healthcare provider will need to monitor you closely for at least 8 weeks, because stopping treatment may cause a breakdown of red blood cells due to PNH, and symptoms such as:

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

What other drugs will affect pegcetacoplan?

Sometimes it is not safe to use certain medications at the same time as pegcetacoplan. Some drugs can affect your blood levels of other drugs you take, which may increase side effects or make the medications less effective. Tell your doctor about all your vaccinations and your medicines, including prescription, over-the-counter, vitamins, and herbal supplements.

Does Pegcetacoplan interact with my other drugs?

Enter medications to view a detailed interaction report using our Drug Interaction Checker.

Storage

Store pegcetacoplan vials in the refrigerator between 36°F to 46°F (2°C to 8°C) in the original carton to protect from light.

Do not use past the expiration date stamped on the carton.

Keep all medicines out of the reach of children and pets.

Pegcetacoplan ingredients

Pegcetacoplan is only available as the brand Empaveli.

Empaveli ingredients

Active ingredient: pegcetacoplan

Inactive ingredients: sorbitol, glacial acetic acid, sodium acetate trihydrate, Water for Injection USP. Pegcetacoplan may also contain sodium hydroxide and/or additional glacial acetic acid for pH adjustment.

Empaveli is available as a subcutaneous injection containing 1080 mg/20mL (54 mg/mL) in a single-dose vial.

Who makes pegcetacoplan?

Pegcetacoplan for infusion is manufactured by Apellis Pharmaceuticals, under the brand name Empaveli. Their headquarters are in Waltham, Massachusetts. Other notable medications by Apellis include:

Popular FAQ

How do Izervay and Syfovre compare?

Izervay (avacincaptad pegol) and Syfovre (pegcetacoplan) are injectable treatments for geographic atrophy (GA), a severe form of age-related macular degeneration (AMD) that causes progressive and irreversible vision loss. Continue reading

How does Empaveli compare to Soliris?

Empaveli is a brand name for pegcetacoplan which is a PEGylated 40kDa polyethylene glycol linear small molecule that acts as a C3 complement inhibitor and Soliris is a brand name for eculizumab which is a monoclonal antibody that specifically binds to the complement protein C5. Empaveli is given by subcutaneous infusion and people can be taught how to self-administer it at home. Soliris is given by infusion under the guidance of a healthcare professional every 2 weeks (after the initial dosing schedule) although most patients are encouraged to switch from Soliris to Ultomaris which only requires 7 infusions in adults a year. Continue reading

How is Empaveli administered?

Empaveli is self-administered subcutaneously (this means under the skin) using the Empaveli on-body autoinjector, or given by a healthcare provider using an infusion pump. The Empaveli injector is a compact, wearable, circular device that is placed on your stomach at least 1 inch from your belly button or previous injection site.

Continue reading
How does Empaveli work?

Empaveli works by targeting the complement system, a key part of our immune system that helps clear damaged cells and fight infections. It binds to complement protein C3, preventing it from splitting into harmful fragments (C3a and C3b).

Continue reading

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.