Home Lilly Halts Phase 1 Trial of Nectin-4 ADC LY4052031 Due to Safety Concerns

Lilly Halts Phase 1 Trial of Nectin-4 ADC LY4052031 Due to Safety Concerns

Apr 25, 2025 08:47 CST Updated 08:47
Eli Lilly

Global Pharmaceutical R&D and Production Company

Eli LillyThe First Clinical Trial of LY4052031Paused Due to Safety Concerns., the companyThe First ClauseLY4101174 is still in clinical trials.

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LY4101174 (ETx-22), acquired from Emergence Therapeutics, which shares the same PSARlink linker and Exatecan payload as LY4170156, also with a DAR of 8. 
LY4052031 uses a GGFG linker with Camptothecin-98 as its payload, achieving a DAR of 8. Both are humanized IgG1 ADCs designed to be Fc-silent.

Nectin-4 is an immunoglobulin-like antigen that is overexpressed in a variety of cancers, including bladder cancer, breast cancer, non-small cell lung cancer, and gastric cancer. Normal tissues express only low to moderate levels of Nectin-4, making this protein an attractive target for cancer therapy.


LY4052031 is a next-generation Nectin-4-targeted ADC developed internally by Eli Lilly.LY4052031The antibody also adopts Fc Silence treatment, with the Payload being the topoisomerase inhibitor Camptothecin-98, and a DAR value of 8.


Preclinical studies have shown that LY4052031 exhibits strong cytotoxicity against tumor cells with both high and low expression of Nectin-4.The product is also available in a variety ofNectin-4Showed strong in vivo efficacy in tumor models expressing and resistant to MMNEOverall, LY4052031, as a next-generation therapy for treating Nectin-4 positive tumors, demonstrates specificity, selectivity, potency, and efficacy.


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Will continue to follow up.


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End


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