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Tezspire (TEZEPELUMAB)

AstraZeneca / Amgen · FDA-approved approved Monoclonal antibody Quality 30/100

Tezepelumab (Tezspire), co-developed by AstraZeneca and Amgen, is a marketed biologic for severe asthma, positioning it in a growing therapeutic segment. Its key strength lies in its unique mechanism of action, which differentiates it from existing treatments. The primary risk is the key composition patent expiry in 2028, which could lead to increased competition from generics and biosimilars.

At a glance

Generic nameTEZEPELUMAB
SponsorAstraZeneca / Amgen
Drug classThymic Stromal Lymphopoietin Blocker [EPC]
ModalityMonoclonal antibody
PhaseFDA-approved
First approval2021

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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