Eli Lilly and Company is ready to file its interleukin-23 inhibitor mirikizumab with the US Food and Drug Administration for approval in moderate-to-severe plaque psoriasis after reporting results from a second successful Phase III study on 17 July. The OASIS-2 trial showed that the candidate was non-inferior to the interleukin-17 inhibitor Cosentyx (secukinumab) on three endpoints at 16 weeks and superior to Novartis AG’s market-leading biologic at 52 weeks on those same endpoints.
Lilly already has its own IL-17 therapy, Taltz (ixekizumab), on the market for psoriasis but the company’s strategy is to...







![Spotlight On RDCs, AOCs As Leading Novel Bioconjugates[Updated]](https://web.insights.norstella-labs.com/resizer/v2/3M7ZAWZOBNK7NG4A4WDOIFG6DU.jpg?smart=true&auth=392a1fdb3cfacb29445720c412410e598dbcc5f90f14857652cd498bd0faa0fb&width=400&height=225)