Condition: Solid Tumor · Advanced Cancer · Metastatic Cancer · Sponsor: I-Mab Biopharma US Limited
The goal of this clinical trial is to learn if givastomig in combination with standard therapy works to treat adults with cancer in the stomach and/or esophagus (GEA adenocarcinoma). It will also help the researchers to learn more about the safety of givastomig. The main questions it aims to answer are: * Does the addition of givastomig to standard therapy increase the amount of time that participants survive without progression of their cancer? * What toxicities do participants experience when taking givastomig? Participants may be able to take part in the study if they have unresectable or metastatic GEA and if their cancer cells express certain proteins called Claudin 18.2 (CLDN18.2) and PD-L1. Participants whose cancer cells express a protein called HER2 cannot take part. Up to 180 participants will be randomly assigned to received givastomig at one of two doses in combination with an immunotherapy medicine called nivolumab and chemotherapy OR to receive nivolumab and chemotherapy alone. These therapies will be given primarily via intravenous (into a vein) infusion every 2 or 3 weeks. Participants will: * Visit the study treatment center for infusions and/or check-ups and tests every 1-3 weeks * Report any changes in their symptoms to their study doctors * Have scans to check for any changes in their cancer every 8-12 weeks
This description comes directly from the study's public registry record.
I-MAB US Clinical Trials · 301-294-4408 · us.info@imabbio.com
Always discuss trial participation with your own doctor first.
| I-Mab Site 1016 | Goodyear, Arizona, United States | Recruiting |
| I-MAB Site 1005 | Duarte, California, United States | Recruiting |
| I-Mab Site 1002 | Boston, Massachusetts, United States | Recruiting |
| I-Mab Site 2001 | Beijing, China | Recruiting |
| I-Mab Site - 4001 | Kashiwa, Japan | Not Yet Recruiting |
| I-Mab Site 4005 | Tokyo, Japan | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07432295