Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
MEDI5752 + axitinib is an experimental combination therapy under clinical investigation for advanced renal cell carcinoma (RCC). MEDI5752 is a bispecific monoclonal antibody targeting both programmed cell death protein 1 (PD-1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), thereby enhancing anti-tumor immune responses by blocking two immune checkpoints simultaneously. Axitinib is an orally administered small molecule tyrosine kinase inhibitor (TKI) that targets vascular endothelial growth factor receptors (VEGFRs), inhibiting angiogenesis and tumor vascularization. The therapeutic rationale for combining these agents is to synergistically enhance anti-tumor immunity and suppress tumor angiogenesis, aiming to improve efficacy in RCC over current immunotherapy or anti-angiogenic monotherapies. This combination is currently being evaluated in phase 1 clinical trials for efficacy and safety in patients with advanced renal cell carcinoma[1][3][4][5][8].
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 MEDI5752 + axitinib.