Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Iodine i 131 tositumomab** is a radioimmunotherapeutic agent used primarily for the treatment of CD20-positive, relapsed or refractory non-Hodgkin's lymphoma. It consists of two components: * **Tositumomab**, a murine IgG2a lambda monoclonal antibody that targets the CD20 antigen on B lymphocytes, and * **Iodine‑131**, a radioactive isotope covalently linked to the antibody. The drug works by binding to CD20 on malignant B cells; this both stimulates immune-mediated cell death and delivers targeted radiation from the attached iodine‑131, resulting in direct cytotoxicity to cancer cells. The regimen involves an initial dosimetric dose followed by a therapeutic dose calculated based on patient-specific factors such as platelet count and biodistribution[2][4][5][7]. Bexxar was developed for patients whose disease is refractory to rituximab and has relapsed following chemotherapy[7]. The product was approved by the FDA but has since been discontinued.
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 tositumomab.