drugset / Trial / NCT03707093

Study of CD137 Agonist ADG106 With Advanced or Metastatic Solid Tumors and/or Non-Hodgkin Lymphoma

NCT03707093

Phase 1 Completed 49 enrolled Adagene Inc
NaSequentialOpen-labelTreatment

Summary

This is a Phase 1, open-label, dose-escalation, multicenter study of ADG106 in subjects with advanced or metastatic solid tumors and/or relapsed/refractory non-Hodgkin lymphoma. ADG106 is a fully human ligand-blocking, agonistic anti-CD137 IgG4 mAb. It binds to the activated human T cells via a T cell receptor CD137. T cell is a kind of lymphocyte (a subtype of white blood cells) that protects bodies by eliminating tumor cells, and normal cells infected with viruses or bacteria. By binding to CD137, the study drug is expected to enhance the activity of activated T cells and thus stimulate a more intense immune attack to kill tumor cells. ADG106 is expected to enhance the activity of activated T cells. The primary objective of the study is to assess safety and tolerability at increasing dose levels of single agent ADG106 in subjects with advanced or metastatic solid tumors and/or non Hodgkin lymphoma Secondary Objectives * To characterize the pharmacokinetic (PK) profiles of ADG106 * To evaluate the immunogenicity of ADG106 * To evaluate the potential anti-tumor effect of ADG106 Exploratory Objective To identify the potential biomarkers of ADG106

Timeline

Start
2018-09-17
Primary completion
2022-01-24
Completion
2022-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject ADG106 Monoclonal antibody 0.03 mg/kg Intravenous
Subject ADG106 Monoclonal antibody 0.1 mg/kg Intravenous
Subject ADG106 Monoclonal antibody 0.3 mg/kg Intravenous
Subject ADG106 Monoclonal antibody 1 mg/kg Intravenous
Subject ADG106 Monoclonal antibody 3 mg/kg Intravenous
Subject ADG106 Monoclonal antibody 10 mg/kg Intravenous
Subject ADG106 Monoclonal antibody 300 mg Intravenous

Indications