Condition: Pancreatic Ductal Adenocarcinoma · Non-small Cell Lung Cancer · Colorectal Cancer · Sponsor: Eli Lilly and Company
The main purpose of the study is to assess whether the study drug, LY4066434, is safe and tolerable when administered to participants with locally advanced or metastatic solid tumors with certain KRAS mutations. LY4066434 will be given alone or in combination with other treatments. The study will have 2 parts: monotherapy dose escalation and dose optimization. The study is expected to last up to approximately 5 years.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| University of Alabama at Birmingham | Birmingham, Alabama, United States | — |
| Mayo Clinic | Phoenix, Arizona, United States | — |
| City of Hope | Duarte, California, United States | — |
| University of California, Los Angeles (UCLA) | Santa Monica, California, United States | — |
| Yale University School of Medicine - Yale Cancer Center | New Haven, Connecticut, United States | — |
| The University of Chicago Medical Center (UCMC) | Chicago, Illinois, United States | — |
| Indiana University (IU) | Indianapolis, Indiana, United States | — |
| Massachusetts General Hospital | Boston, Massachusetts, United States | — |
| Dana-Farber Cancer Institute | Boston, Massachusetts, United States | — |
| South Texas Accelerated Research Therapeutics (START) Midwest | Grand Rapids, Michigan, United States | — |
| Columbia University | New York, New York, United States | — |
| David H. Koch Center for Cancer Care at Memorial Sloan Kettering Cancer Center | New York, New York, United States | — |
+ 33 more locations — full list on the registry record.
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