Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Neuradiab + temozolomide is a combination regimen used in the adjuvant treatment of glioblastoma multiforme (GBM). Neuradiab is a radiolabeled monoclonal antibody (anti-tenascin-C, murine 81C6) conjugated to iodine-131, locally administered into the surgical resection cavity after removal of GBM. It delivers targeted radioactivity to residual tumor cells by binding tenascin-C, which is overexpressed in GBM and absent in normal brain cells. Temozolomide is an oral alkylating agent administered systemically as a standard chemotherapeutic component of GBM treatment. The combination is designed to maximize killing of residual tumor cells through a dual modality: local radioimmunotherapy from Neuradiab targeting tenascin-C and systemic chemotherapy from temozolomide. The combination has been studied, primarily in newly diagnosed GBM, with Neuradiab provided as an adjuvant to surgery, external beam radiation, and temozolomide. Development was mainly by Bradmer Pharmaceuticals and Duke University, with Phase 3 trials conducted but ultimately terminated[1][2][3][6].
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 Neuradiab + temozolomide.