Clinical ProgressThe company's lead asset, Temferon, is advancing in first-line glioblastoma and has expanded into metastatic renal cell carcinoma, showing progress in its clinical programs.
Regulatory ApprovalGenenta recently received approval from the Agenzia Italiana del Farmaco (AIFA) to initiate this Phase 1 study in mRCC.
Safety ProfileIn the Phase 1/2a trial for glioblastoma, Temferon has been well tolerated with no dose-limiting toxicities, highlighting its safety profile.