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Tezspire

Pronunciation: TEZ-SPY-ER
Generic name: tezepelumab-ekko
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 Sep 5, 2023.

What is Tezspire?

Tezspire (Tezepelumab-ekko) is an add-on, injectable treatment that can be self-administered under the skin every 4 weeks 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. It can help prevent severe asthma attacks and improve breathing but is not a rescue medication and will not relieve acute bronchospasm or status asthmaticus.

Tezspire 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.

How does Tezspire 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. Tezspire blocks the action of TSLP, which reduces inflammation and prevents asthma attacks, although the exact way Tezspire works in asthma is not known.

Tezspire was FDA approved on December 17, 2021.

Warnings

Tezspire may cause hypersensitivity reactions, such as a rash and allergic conjunctivitis) and severe reactions including anaphylaxis have also been reported. Appropriate treatment should be initiated if a reaction occurs.

Abrupt reductions in corticosteroid dosage may be associated with systemic withdrawal symptoms and/or unmask conditions previously suppressed by systemic corticosteroid therapy. Decrease corticosteroids gradually, if appropriate.

TSLP may be involved in the immunological response to some helminth (worm and parasitic) infections. Treat patients' pre-existing helminth infections before starting treatment with Tezspire. If a patient develops a helminth infection during treatment that does not respond, discontinue Tezspire until the infection resolves.

Avoid using live attenuated vaccines in patients receiving Tezspire.

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

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

Who should not receive Tezspire?

You should not receive Tezspire 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 Tezspire during pregnancy but it is known placental transfer of monoclonal antibodies such as tezepelumab-ekko 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-ekko in human milk, its effects on the breastfed infant, or its effects on milk production.

Before receiving Tezspire

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

How will I receive Tezspire?

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

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

Each Tezspire 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 Tezspire pen:

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 Tezspire 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 are the side effects of Tezspire?

Tezspire may cause serious side effects, including:

The most common side effects occurring in more than 3% of people include:

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.

What other drugs will affect Tezspire?

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 Tezspire. Refer to the product information for any updates.

What are the ingredients in Tezspire?

Active ingredient: tezepelumab-ekko. Available as:

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

Storage

Store Tezspire 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 Tezspire 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 Tezspire pre-filled pen and all medicines out of the sight and reach of children

Manufacturer

Amgen Inc. and AstraZeneca.

Popular FAQ

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.