A Study of DXC014 in Patients With Advanced Solid Tumors.
This is a phase I, open-label, first-in-human clinical study designed to evaluate the safety, tolerability, MTD, DLT, RP2D, the PK characteristics, preliminary anti-tumor activity, the immunogenicity of DXC014 in patients with Advanced Solid Tumors.
Voluntarily sign the informed consent form and comply with the protocol requirem... [+2]
Within 14 days prior to the first dose: Underwent plasmapheresis; received syste... [+17]