Lilly Dual Agonist Ph3 Analysis; EASD Investor Presentation

Following Lilly’s Ph2b data presentation for its GIP/GLP-1RA dual agonist (LY3298176), the company hosted an analyst call (slides here) to discuss the data. Of note, Lilly outlined its Ph3 development program called “SURPASS” (pictured below) which includes a H2H study vs. semaglutide. Lilly is planning to initiate Ph3 in late 2018 or early 2019 and is projecting global submissions in 2022. Additionally, Lilly disclosed that it will bring the 5, 10, and 15mg doses into Ph3 and will use an auto-injector device. Earlier today, FENIX outlined the LY Ph2b results and provided the potential impact to Novo Nordisk and Sanofi. Below, FENIX conducted a comparative analysis on contemporary Ph3 GLP-1RA pivotal programs, potential rationales behind Lilly’s Ph3 study choices, and how the LY dual agonist is a pipeline-in-a-product similar to Novo’s semaglutide.

About The Author

Matthew Maryniak

President of Fenix Group International

Matthew has been a thought leader in the high-growth therapeutic areas of diabetes and cardiovascular medicine since 2006, making regular attendance at large and small CV/met scientific meetings and an architect of novel methods for assessing market opportunities. He has over a decade of experience in leading CV/met consulting engagements, is a published author in PM360 and Diabetes Technology & Therapeutics, and has been quoted in The Pink Sheet on anti-thrombotics.

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