With regulatory approval for a broader label pending in the USA, Eli Lilly (NYSE: LLY) has released more data on psoriatic arthritis candidate Taltz (ixekizumab) supporting the efficacy of the IL-17A inhibitor.
Data presented orally at EULAR, the Annual European Congress of Rheumatology, currently underway in Madrid, show that patients who had inadequate response or were intolerant to TNF inhibitors achieved significant improvement at 24 weeks.
Lilly has applied to extend the marketable application of Taltz in the USA, to include treatment of adult patients with active PsA. It is approved for this indication in Japan.
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