About this trial

This is a study of LY4337713 in participants with certain types of cancer that is advanced or has spread. Participants must have cancer with high levels of a protein called fibroblast activation protein (FAP). The purpose of this study is to evaluate safety, side effects, and efficacy of LY4337713. In addition, this study will evaluate how much LY4337713 gets into the bloodstream, how it is broken down, and how long it takes the body to get rid of it. For each participant, the study will last about 5 years.

Eligibility criteria

Qualifiers

Must have clinical or imaging evidence of fibroblast activation protein (FAP) expression per local assessment

Adenocarcinoma of the pancreas

Hormone receptor (HR)-positive human epidermal growth factor 2 (HER2)-negative breast cancer

HER2-positive breast cancer

Disqualifiers

Have known active central nervous system (CNS) metastases or carcinomatous meningitis.

Have significant cardiovascular disease

Have prolongation of the corrected QTcF >470 milliseconds (msec) during screening. QTcF is calculated using Fridericia's Formula: QTcF = QT/(RR0.33)

Have evidence of ongoing and untreated urinary tract obstruction

Trial design

Treatments tested in this trial

  • LY4337713

Treatment groups

241 Participants
are divided into 6 treatment groups

6

Treatment groups

See each treatment group below.

Locations

30
China
Fudan University Zhongshan Hospital200032, Shanghai China
Germany
Universitaetsklinikum Essen45147, Essen Germany
Japan
National Cancer Center Hospital East277-8577, Chiba Japan
Kyoto University Hospital606-8507, Kyoto Japan

Sponsors and collaborators

Eli Lilly and Company

Lead sponsor