Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Iodine I-131 girentuximab** is an investigational CAIX-directed radioimmunotherapy for metastatic clear-cell renal cell carcinoma. It consists of the chimeric IgG1 monoclonal antibody girentuximab, also known as cG250, covalently radiolabeled with iodine-131. The antibody binds carbonic anhydrase IX on clear-cell renal carcinoma cells, concentrating iodine-131 beta radiation at CAIX-positive tumor sites and causing localized radiation-induced DNA damage and tumor-cell death. Phase I and II studies evaluated single and fractionated intravenous administrations in advanced metastatic renal cell carcinoma; hematologic toxicity, particularly thrombocytopenia, was dose-limiting, and the program did not become a marketed therapy. ([pubmed.ncbi.nlm.nih.gov](https://pubmed.ncbi.nlm.nih.gov/16203819/))
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on iodine i-131 girentuximab.