A first-in-human Phase I non-randomized open-label multicenter dose escalation trial of BI 765049 and BI 765049 + ezabenlimab administered by parenteral administration(s) in patients with malignant solid tumors expressing B7-H6
Are you eligible to participate in this study?
You may be eligible for this study if you meet the following criteria:
-
Conditions: Malignant Solid Tumors Expressing B7-h6
-
Age: Between 18 Year(s) - 100 Year(s)
-
Gender: Male or Female
-
Other Inclusion Criteria:
- Patients with a histologically or cytologically confirmed diagnosis of an advanced, unresectable, and/or metastatic colorectal carcinoma (CRC), non-small cell lung cancer (NSCLC), hepatocellular carcinoma (HCC), head and neck squamous cell carcinoma (HNSCC), gastric carcinoma, and pancreatic carcinoma
- Patients with disease progression despite conventional treatment, intolerant to or not a candidate for conventional treatment, or with a tumor for which no conventional treatment exists
- Patient diagnosed with advanced or metastatic CRC or patient with confirmed B7-H6 expression on tumor tissue sample (archived or fresh tumor biopsy) based on central pathology review
You may not be eligible for this study if the following are true:
-
- Patient with a history of a major surgery within 28 days prior to first dose of BI 765049
- Patient with a history of a previous or concomitant malignancies
- Patient with known leptomeningeal disease or spinal cord compression due to disease
If you are registered as a volunteer, please log in to contact the study team/express interest in this study.