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Taltz ® (ixekizumab) injection
80 mg/mLThis information is provided in response to your request. Resources may contain information about doses, uses, formulations and populations different from product labeling. See Prescribing Information above, if applicable.
For the analyses summarized below, response was defined as a sPGA score of 0 (clear skin) or 1 (minimal) and relapse was defined as a sPGA score of >3.1
In 2 phase 3 clinical trials, patients who were originally randomized to ixekizumab and who responded to treatment at week 12 were re-randomized to an additional 48 weeks of ixekizumab 80 mg Q4W or placebo.1
In those week 12 responders to ixekizumab who were re-randomized to treatment withdrawal (ie, placebo), 7% maintained their clinical response at week 60. The median time to relapse was 164 days.1
In responders who were re-randomized to treatment with ixekizumab Q4W, 75% maintained their response at week 60.1
Enclosed Prescribing Information
TALTZ® (ixekizumab) injection, for subcutaneous administration, Lilly
1. Taltz [package insert]. Indianapolis, IN: Eli Lilly and Company; 2020.
Glossary
Q4W = every 4 weeks
sPGA = static Physician Global Assessment
Date of Last Review: September 17, 2018
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