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Pyzchiva

Pronunciation: piz-chi-va
Generic name: ustekinumab-ttwe
Dosage form: subcutaneous injection single-dose prefilled syringe (45 mg/0.5 mL or 90 mg/mL), injection for intravenous Infusion single-dose vial 130 mg/26 mL (5 mg/mL)
Drug class: Interleukin inhibitors

Medically reviewed by Carmen Pope, BPharm. Last updated on Jul 3, 2024.

What is Pyzchiva?

Pyzchiva (ustekinumab-ttwe) is an injectable human interleukin-12 and 23 blocker which is a biosimilar to Stelara that may be used to treat certain types of plaque psoriasis, active psoriatic arthritis, Crohn’s disease, and ulcerative colitis, which are all autoimmune conditions.

Pyzchiva works by blocking certain inflammatory proteins in your body, called IL-12 (interleukin-12) and IL-23 (interleukin-23). These proteins are known as cytokines and they are responsible for the inflammation associated with certain autoimmune conditions. By blocking their activity, Pyzchiva reduces inflammation, pain, swelling, and skin symptoms.

For people with Crohn's disease and ulcerative colitis, a healthcare provider usually gives the first injection of Pyzchiva as an infusion into a vein in their arm. Subsequent injections are given by injection under the skin (subcutaneous [SC] injection). Patients with psoriasis or psoriatic arthritis will receive all doses of Pyzchiva as an SC injection. 

Pyzchiva was FDA-approved on June 28, 2024, as a biosimilar to Stelara. A biosimilar is a biological product that is like the reference biologic (in this case Stelara) and for which there are no clinically meaningful differences in terms of safety, purity, and potency. An interchangeable biosimilar can be substituted for the reference product at the pharmacy level, without contacting the prescriber, subject to state laws. Interchangeable biosimilars to Stelara include Wezlana.

What is Pyzchiva used for?

Pyzchiva is FDA-approved to treat:

Pyzchiva side effects

Common Pyzchiva side effects may include:

Serious Pyzchiva side effects and warnings

Get emergency medical help if you have signs of an allergic reaction to Pyzchiva, such as hives; chest pain, difficulty breathing; feeling light-headed; or swelling of your face, lips, tongue, or throat.

Serious infections may occur during treatment with Pyzchiva. People who have a genetic problem where the body does not make any of the proteins interleukin 12 (IL-12) and interleukin 23 (IL-23) are at a higher risk for certain serious infections. These infections can spread throughout the body and cause death. Call your doctor right away if you have signs of infection such as fever, chills, muscle pain, shortness of breath, weight loss, diarrhea or stomach pain, burning when you urinate, feeling very tired, skin warmth or redness, painful skin sores, or coughing up blood.

Pyzchiva may cause a rare but serious condition affecting the brain called Posterior Reversible Encephalopathy Syndrome (PRES). Tell your doctor right away if you have a headache, confusion, vision problems, or a seizure.

Pyzchiva may decrease the activity of your immune system, and there may be an increase in your risk for certain types of cancers. Tell your doctor if you have ever had any type of cancer. Some people who are receiving this medicine and have risk factors for skin cancer have developed certain types of skin cancers. During your treatment with this medicine, tell your doctor if you develop any new skin growths.

Also, call your doctor at once if you have:

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or to Sandoz Inc. at 1-800-525-8747. 

Before taking this medicine

You should not use Pyzchiva if you:

Before you start treatment with this injection, your doctor may perform tests to make sure you do not have tuberculosis.

To make sure Pyzchiva is safe for you, tell your doctor if you:

Some people using this medicine have developed skin cancer (non-melanoma). However, these people may have had a higher risk of skin cancer. Talk to your doctor about this risk and what skin symptoms to watch for. You may need to have regular skin exams.

Pregnancy

It is not known whether this medicine will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant. If you are pregnant, your name may be listed on a pregnancy registry to track the effects of ustekinumab on the baby.

Breastfeeding

It may not be safe to breastfeed while using this medicine. It is thought that Pyzchiva passes into your breast milk in small amounts. Talk to your doctor about the best way to feed your baby if you receive this medicine.

How should I use Pyzchiva?

Follow all directions on your prescription label and read all medication guides or instruction sheets. Use the medicine exactly as directed.  Pyzchiva is intended for use under the guidance and supervision of your doctor. Prepare your injection only when you are ready to give it. Do not use it if the medicine looks cloudy, has changed colors, or has particles in it. Call your pharmacist for new medicine.

Crohn’s disease and ulcerative colitis the first dose of Pyzchiva is given through a vein in the arm (intravenous infusion) in a healthcare facility by your healthcare provider. It takes at least 1 hour to receive the infusion. Your next doses will be given as an injection under the skin (subcutaneous injection).

Psoriasis or psoriatic arthritis Pyzchiva is given as an injection under the skin (subcutaneous injection) as described below.

Injecting Pyzchiva under your skin

Pyzchiva dosing information

The dosage of Pyzchiva is dependent on the patient's weight. Your healthcare provider will calculate this for you.

Crohn’s disease and ulcerative colitis: Pyzchiva is given as an infusion for the first dose then as a subcutaneous injection every 8 weeks thereafter. 

Psoriasis and Psoriatic Arthritis: Pyzchiva is given as a subcutaneous injection initially and 4 weeks later, then a dose is given every 12 weeks.

Pyzchiva is available as:

Subcutaneous Injection

Intravenous Infusion 

What happens if I miss a dose?

Call your doctor for instructions if you miss a dose.

What happens if I overdose?

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

What should I avoid while using Pyzchiva?

Avoid being near people who are sick or have infections. Tell your doctor at once if you develop signs of infection.

Do not receive a "live" vaccine while using this medicine, and avoid coming into contact with anyone who has recently received a live vaccine. There is a chance that the virus could be passed on to you. Live vaccines include measles, mumps, rubella (MMR), rotavirus, typhoid, yellow fever, varicella (chickenpox), zoster (shingles), and nasal flu (influenza) vaccine.

BCG vaccine should not be given for at least 1 year after you receive your last dose of Pyzchiva.

Non-live vaccines (including flu shots) may not work as well during your treatment, and may not fully protect you from disease. Make sure you are current on all vaccines before you begin treatment with this medicine.

What other drugs will affect Pyzchiva?

Other drugs may interact with Pyzchiva, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell your doctor about all your current medicines and any medicine you start or stop using.

It is important to tell your doctor if you are taking any of the following: 

Your doctor may need to change the doses of your medications or monitor you carefully for side effects. Not all possible interactions are listed here.

Storage

Pyzchiva vials and prefilled syringes

Pyzchiva Ingredients

Active ingredient: ustekinumab-ttwe

Inactive ingredients: 

Single-dose prefilled syringe for subcutaneous use: histidine, histidine hydrochloride monohydrate, polysorbate 80, and sucrose.

Single-dose vial for intravenous infusion: edetate disodium, histidine, histidine hydrochloride monohydrate, methionine, polysorbate 80, and sucrose. 

Who makes Pyzchiva?

Samsung Bioepis Co., Ltd., makes Pyzchiva for Sandoz Inc. 

Frequently asked questions

Further information

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