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Clinical Trials associated with DXC-006 / Not yet recruitingPhase 1/2 A Phase Ib/II Study to Evaluate the Safety and Efficacy of DXC006 for Injection Combined With Immune Checkpoint Inhibitors or Platinum-Based Agents in Patients With Small Cell Lung Cancer.
This is a Phase Ib/II, open-label clinical study designed to evaluate the safety, tolerability, preliminary anti-tumor activity, recommended Phase 2 dose (RP2D), pharmacokinetic (PK) characteristics, and immunogenicity of DXC006 in combination with an immune checkpoint inhibitor (ICI) or platinum-based chemotherapy in patients with small cell lung cancer (SCLC).
An Open-label Dose Escalation and Cohort Expansion Phase I Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics and and Efficacy of DXC006 in Patients With Advanced Solid Tumors and Hematologic Malignancies
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 DXC006 in patients with a variety of solid tumors, including small cell lung cancer, multiple myeloma, and neuroblastoma, and hematological malignancies.
/ Not yet recruitingPhase 1IIT An open-label dose escalation and cohort expansion phase I clinical trial to evaluate the safety, tolerability, pharmacokinetic characteristics and and efficacy of DXC006 in patients with advanced solid tumors and hematologic malignancies
100 Clinical Results associated with DXC-006
100 Translational Medicine associated with DXC-006
100 Patents (Medical) associated with DXC-006
100 Deals associated with DXC-006