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Taltz (ixekizumab)

Eli Lilly · FDA-approved approved Monoclonal antibody Verified Quality 82/100

Humanized IgG4 monoclonal antibody that selectively binds IL-17A cytokine and inhibits its interaction with IL-17 receptor.

Ixekizumab (Taltz) is a humanized IgG4 monoclonal antibody antagonist of IL-17A indicated for moderate-to-severe plaque psoriasis (ages 6+), psoriatic arthritis, ankylosing spondylitis, and non-radiographic axial spondyloarthritis in adults. The drug demonstrates favorable pharmacokinetics with a 13-day half-life, achieves steady-state by Week 8, and exhibits dose-proportional kinetics with bioavailability of 60-81% following subcutaneous injection. Common adverse reactions include injection site reactions (17%), upper respiratory tract infections (14%), nausea (2%), and tinea infections (2%), with serious adverse events occurring in 2% of treated subjects. The primary safety concern is infection risk, requiring monitoring and contraindication in patients with serious hypersensitivity reactions to the drug or its excipients.

At a glance

Generic nameixekizumab
SponsorEli Lilly
Drug classInterleukin-17A antagonist
TargetInterleukin 17A (IL-17A) cytokine
ModalityMonoclonal antibody
Therapeutic areaImmunology
PhaseFDA-approved
First approval2016
Annual revenue2700

Mechanism of action

Ixekizumab is a humanized IgG4 monoclonal antibody that selectively binds to interleukin 17A (IL-17A), a naturally occurring cytokine involved in normal inflammatory and immune responses. By binding to IL-17A, ixekizumab inhibits the interaction between IL-17A and the IL-17 receptor, thereby blocking a key pathway in inflammatory signaling. This mechanism results in the inhibition of the release of proinflammatory cytokines and chemokines, reducing the inflammatory response in conditions such as plaque psoriasis, psoriatic arthritis, ankylosing spondylitis, and non-radiographic axial spondyloarthritis.

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
SEC EDGARRevenue + earnings