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Tezepelumab

Pronunciation: tez-e-pell-u-mab
Generic name: tezepelumab-ekko
Brand name: Tezspire
Dosage forms: subcutaneous pre-filled pen, subcutaneous pre-filled syringe, injection, for subcutaneous use
Drug class: Selective immunosuppressants

Medically reviewed by Carmen Pope, BPharm. Last updated on Nov 1, 2024.

What is tezepelumab?

Tezepelumab is used for the maintenance treatment of severe asthma in people 12 years of age and older, whose asthma is not controlled with their current asthma medicine. Tezepelumab injection is self-administered under the skin every 4 weeks and is used in addition to other asthma treatments.

Tezepelumab is a thymic stromal lymphopoietin (TSLP) blocker, human monoclonal antibody IgG2λ. It is the only biologic approved for severe asthma with no phenotype (ie, eosinophilic or allergic) or biomarker limitation within its approved label. It can help prevent severe asthma attacks and improve breathing but is not a rescue medication and will not relieve acute bronchospasm or status asthmatics.

How does tezepelumab work?

Airway inflammation is a significant component of Asthma. When you encounter a trigger, your lungs release multiple substances, including thymic stromal lymphopoietin (TSLP), a cytokine expressed mainly by epithelial cells, that is one of the first substances to be released. Tezepelumab's mechanism of action involves blocking the action of TSLP, which reduces inflammation and prevents asthma attacks, although the exact way tezepelumab works in asthma is not known.

Tezepelumab gained FDA approval on December 17, 2021 under the brand name Tezspire. There is no Tezspire generic or biosimilar. The full biological name of tezepelumab is tezepelumab-ekko.

Tezepelumab side effects

The most common side effects of tezepelumab are:

Weight gain has not been reported as a side effect of tezepelumab.

Serious side effects and warnings

Tezepelumab injection may cause allergic reactions, such as a rash and allergic conjunctivitis. Severe reactions including anaphylaxis have also been reported. Call your healthcare provider or get emergency medical care if you get any of the following symptoms of an allergic reaction:

Abrupt reductions in corticosteroid dosage may be associated with systemic withdrawal symptoms and/or unmask conditions previously suppressed by systemic corticosteroid therapy. Your healthcare provider will taper off your corticosteroid dose gradually, if appropriate.

The cytokine TSLP involved with tezepelumab's mechanism of action may be involved in the immunological response to some helminth (worm and parasitic) infections. If you have a worm or parasite infection it should be treated before starting treatment with tezepelumab. If you develop a worm or parasite infection during treatment that does not respond, your healthcare provider may temporarily discontinue your tezepelumab injection until the infection resolves.

You should avoid receiving a live attenuated vaccine (such as a measles, chickenpox, or rotavirus vaccine) while you are receiving tezepelumab injections.

Tell your healthcare provider if your asthma does not get better or if it gets worse after you start treatment with tezepelumab.

It is not known if this medicine is safe and effective in children under 12 years of age.

See What are 5 key Tezspire side effects to watch out for? for more detailed information.

These are not all of the possible side effects. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

Who should not receive tezepelumab?

You should not receive tezepelumab if you are allergic to tezepelumab or any of the other ingredients. See the end of this page for a complete list of ingredients.

There is no available data on the use of tezepelumab injection during pregnancy but it is known placental transfer of monoclonal antibodies such as tezepelumab is greater during the third trimester of pregnancy. Consider risks versus benefits including disease-associated maternal and/or embryo/fetal risk in women with poorly or moderately controlled asthma (such as increased risk of preeclampsia, and prematurity, low birth weight, and small for gestational age in the neonate.

There is no information regarding the presence of tezepelumab in human milk, its effects on the breastfed infant, or its effects on milk production.

Before receiving tezepelumab

Before you receive tezepelumab, tell your healthcare provider about all of your medical conditions, including if you:

How will I receive tezepelumab?

Tezepelumab injection is available as a vial, a pre-filled syringe, and a prefilled pen. Each contains a single dose of tezepelumab.

The usual dosage of tezepelumab is 210mg (one vial/syringe/pen) administered under your skin (subcutaneously) once every 4 weeks.

Each tezepelumab pre-filled pen contains 1 dose that can only be used 1 time. It can only be given as an injection under the skin (subcutaneous).

To use the tezepelumab pen:

See How do I use the Tezspire Pen? for more detailed information.

Tezspire, prednisone, Breo Ellipta, Dupixent, Xopenex, Atrovent, Dulera

What happens if I miss a dose?

If you miss an appointment, ask your healthcare provider when to schedule your next treatment.

If you are self-administering tezepelumab and you miss a dose, inject the dose as soon as you can. Ring your healthcare provider for more information.

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 tezepelumab?

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Do not change or stop your corticosteroid medicines or other asthma medicines unless your healthcare provider tells you to.

No formal drug interaction studies have been performed with tezepelumab. Refer to the product information for any updates.

Does tezepelumab interact with my other drugs?

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

What are the ingredients in tezepelumab?

Tezepelumab is only available as the brand name Tezspire.

Active ingredient: tezepelumab-ekko. Available as:

Inactive ingredients: glacial acetic acid, L-proline, polysorbate 80, sodium hydroxide, and water for injection

Storage

Store tezepelumab in a refrigerator between 36°F to 46°F (2°C to 8°C) in its original carton to protect it from light until you are ready to use it.

It may be kept at room temperature between 68°F to 77˚F (20°C to 25°C) for a maximum of 30 days. Do not return to the refrigerator, instead discard it if it has not been used within this time.

Do not use your tezepelumab pre-filled pen if:

Do not:

If any of the above happens, throw away the pre-filled pen in a puncture-resistant (sharps) container and use a new pre-filled pen.

Keep the tezepelumab pre-filled pen and all medicines out of the sight and reach of children

Who makes tezepelumab?

Amgen Inc. and AstraZeneca make tezepelumab under the brand name Tezspire.

Tezepelumab Biosimilars

Biosimilar and interchangeable products are biological products that are highly similar to and have no clinically meaningful differences from the reference product.

Reference products

These are biological products that have already been approved by the FDA, against which biosimilar products are compared. There is 1 for tezepelumab.

Tezspire (tezepelumab-ekko) - AstraZeneca AB
Formulation type Strength
Autoinjector 210 mg/1.91 mL (110 mg/mL)
Pre-Filled Syringe 210 mg/1.91 mL (110 mg/mL)
Single-Dose Vial 210 mg/1.91 mL (110 mg/mL)

View Tezspire information in detail.

Popular FAQ

How do I use the Tezspire pen?

Your healthcare provider can show you how to self-administer the Tezspire pen. Do not attempt to administer it yourself until you have received full instructions. Take it out of the refrigerator, and leave it in the carton and allow it to come to room temperature between 68°F to 77˚F (20°C to 25°C) for about 60 minutes before giving the injection. Do not remove the cap just yet. Continue reading

Further information

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