Summary
This is a phase I/Ib, first-in-human (FIH), open-label, dose escalation and dose
expansion study to evaluate the safety and tolerability, biological and clinical
activities of GEN-001 in patients with locally advanced or metastatic solid tumors who
have progressed on at least two lines of approved therapy for their histological subtypes
which includes an anti-PD-1 or anti-PD-L1 based therapy (as mono or combination), when
administered as combined with avelumab.