Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Rilotumumab + mitoxantrone + prednisone** is an investigational combination regimen evaluated for the treatment of castration-resistant prostate cancer, especially in patients who are refractory to taxane-based chemotherapy. **Rilotumumab** is a fully human monoclonal antibody targeting hepatocyte growth factor (HGF), thereby inhibiting the HGF/c-MET pathway, which is involved in tumor cell proliferation and survival. **Mitoxantrone** is a cytotoxic anthracenedione antineoplastic agent that intercalates into DNA and inhibits topoisomerase II, leading to DNA damage and cell death. **Prednisone** is a synthetic corticosteroid that is used for its anti-inflammatory and immunosuppressive properties and as a palliative agent in prostate cancer to reduce symptoms and tumor-related complications. This triplet combination was studied in multicenter, randomized phase II trials. Although well tolerated, it did not show a significant improvement in overall survival or progression-free survival versus mitoxantrone and prednisone alone[1][2][3][4].
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 rilotumumab + mitoxantrone + prednisone.