Olomorasib with cetuximab and chemotherapy for advanced colorectal cancer with a KRAS G12C mutation
Tests olomorasib plus other drugs in adults with advanced KRAS G12C colorectal cancer.
Plain-language title generated from the registry record
Registry title: A Study of Olomorasib (LY3537982) in Participants With Advanced Colorectal Cancer and a KRAS G12C Mutation
Key facts
- Where
- Beijing, ChinaSee the site
- Phase
- Phase 2
AI summary: who the study is looking for
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with colorectal cancer that has a KRAS G12C change and cannot be removed by surgery or has spread.
- Age
- 18 years and older.
- Sex
- All sexes can join.
- Disease stage
- Colorectal cancer, Stage III or Stage IV, that cannot be treated with radical surgery or radiation meant to remove all of the disease. The disease must be measurable (RECIST v1.1). Activity level (ECOG) of 0 or 1.
- Earlier treatment
- No earlier treatment for cancer that has spread. 1-2 cycles of FOLFOX before joining are allowed when treatment is needed right away.
- Biomarker or test result
- Evidence of a KRAS G12C mutation is required.
Main reasons for not taking part
- Known BRAF V600E mutation
- Confirmed MSI-H/dMMR
- Active inflammatory bowel disease or a condition that affects absorption of oral drugs
- Untreated active cancer in the brain or its linings
- Pregnant or breastfeeding, or planning pregnancy during the study
Read by machine on 9 November 2026.
Where in China
- Beijing Cancer HospitalBeijing, ChinaNo longer taking part
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- Eli Lilly and Company
- Trial code
- NCT07814417EU 2026-526138-23-00
- Record updated
- 15 October 2026
- Original description
The main purpose of this study is to evaluate how well olomorasib is tolerated and what side effects may occur when combined with other interventions in participants with Kirsten rat sarcoma viral oncogene homolog (KRAS) G12C-mutant, locally advanced colorectal cancer (CRC) that cannot be removed with surgery or has spread to other parts of the body. Blood tests will be performed to investigate how the body processes the study drug.Read full original descriptionShow less
A Phase 2, Open-Label Study to Evaluate the Safety and Efficacy of Olomorasib in Combination With Cetuximab and mFOLFOX6 in Participants With KRAS G12C-Mutant, Locally Advanced Unresectable or Metastatic Colorectal Cancer
The main purpose of this study is to evaluate how well olomorasib is tolerated and what side effects may occur when combined with other interventions in participants with Kirsten rat sarcoma viral oncogene homolog (KRAS) G12C-mutant, locally advanced colorectal cancer (CRC) that cannot be removed with surgery or has spread to other parts of the body. Blood tests will be performed to investigate how the body processes the study drug.
Inclusion: Histologically or cytologically confirmed colorectal cancer (CRC) with Stage III or Stage IV disease, not suitable for curative intent radical surgery or radiation therapy; Must have disease with evidence of KRAS G12C mutation; Have measurable disease per RECIST v1.1; Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1; Ability to swallow capsules; Have adequate laboratory parameters; Have not received treatment for their CRC that has spread to other parts of the body; 1-2 cycles of FOLFOX prior to study enrollment will be allowed for cases where immediate treatment is clinically indicated.
Exclusion: Have active inflammatory bowel disease requiring immunosuppressive medication or previous clear history of inflammatory bowel disease; Have known positive Immunoglobulin E (IgE) antibodies against galactose-α-1,3-galactose (alpha-gal); Have received adjuvant, neoadjuvant, concurrent chemoradiotherapy, or consolidation therapy if treatment was completed less than 6 months prior to enrollment; Have a clinically significant active malabsorption syndrome or other conditions likely to affect gastrointestinal absorption of the orally administered study treatments; Have known additional malignancy that is progressing or has required treatment within the past 2 years; Have uncontrolled, significant cardiovascular disease or cerebrovascular disease; Have an active fungal, bacterial, or active, untreated viral infection; Have human immunodeficiency virus (HIV) with a history of Kaposi's sarcoma or Multicentric Castleman's Disease; Have known untreated active central nervous system metastases or carcinomatous meningitis; Have known B-Raf proto-oncogene, serine/threonine kinase (BRAF) V600E gene mutation; Have confirmed Microsatellite Instability-High/deficient Mismatch Repair (MSI-H/dMMR); Individuals with known low or absent dihydropyrimidine dehydrogenase activity; Are pregnant, breastfeeding, or intend to become pregnant during the study.