Eli Lilly is building on its small drug molecule portfolio with a partnership with Prism Biolab to develop and commercialise small molecules that modulate targets picked by Lilly.
As part of the agreement, Prism will receive upfront payments and up to $660m based on preclinical, clinical, and commercial development milestone payments, along with royalty payments. This alliance will utilise Prism’s PepMetics technology platform to discover oral protein-protein interaction (PPI) targets.
Lilly has made several moves in the last couple of years to develop small-drug molecules. Earlier this month, the company was one of the investors in Alto Neuroscience’s $45m Series C financing round, which will support Alto’s clinical programme of four small-molecule CNS candidates to treat psychiatric disorders including depression and post-traumatic stress disorder.
Alto is expecting positive topline data from Phase II studies investigating two of the molecules, ALTO-100 and ALTO-300, in H2 2024 and H1 2025, respectively.
In December 2022, Lilly signed a partnership with Tokyo-based Sosei for the development of small molecules that modulate new G protein-coupled receptor (GPCR) targets linked to diabetes and metabolic diseases.
Lilly has a number of its own small molecules in development. One of them the selective estrogen receptor degrader (SERD) LY-3484356 (imlunestrant tosylate), is being studied for the treatment of estrogen receptor-positive and HER2-negative metastatic breast cancer, breast cancer and endometrial cancer, in six Phase III trials. The revenue for LY-3484356 is expected to reach an annual total of $112m by 2034 in the US based on GlobalData’s expiry model.
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By GlobalDataGlobalData is the parent company of Pharmaceutical Technology.
In the announcement accompanying the partnership, Prism president and chief executive officer Dai Takehara said: “Our PepMetics technology holds promise to change the current paradigm in drug discovery by turning previously undruggable PPIs into targets readily druggable with small molecules.â€
Eli Lilly has taken several hits this year having received three complete response letters (CRL) from the FDA, and reporting a net loss of $57.4m in Q3 2023. The most recent CRL pertained to Lilly’s lebrikizumab for atopic dermatitis or eczema while the prior two letters dealt with Omvoh (mirikizumab) and donanemab.