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Clinical Trial Summary

The purpose of this study is to find out whether the study drug, LY4101174, is safe, tolerable and effective in participants with advanced, or metastatic solid tumors. The study is conducted in two parts - phase Ia (dose-escalation, dose-optimization) and phase Ib (dose-expansion). The study will last up to approximately 4 years.


Clinical Trial Description

This is a Phase 1a/1b multicenter, open-label study in participants with advanced or metastatic solid tumor malignancies known to express Nectin 4. This study is comprised of two phases: Dose Escalation and Dose Optimization (1a), and Dose expansion (1b). Phase 1a will assess the safety, tolerability, and pharmacokinetics of LY4101174 to determine the recommended phase 2 dose (RP2D)/optimal dose. Phase 1b will evaluate efficacy and safety of LY4101174 at the RP2D/optimal dose in 7 expansion cohorts based on tumor type and/or treatment history. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06238479
Study type Interventional
Source Eli Lilly and Company
Contact Patient Advocacy
Phone 855-569-6305
Email clinicaltrials@loxooncology.com
Status Recruiting
Phase Phase 1
Start date March 5, 2024
Completion date March 4, 2027

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