drugset / Trial / NCT03489343

Sym023 (Anti-TIM-3) in Patients With Advanced Solid Tumor Malignancies or Lymphomas

NCT03489343

Phase 1 Completed 24 enrolled Symphogen A/S
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This was the first study to test Sym023 in humans. The primary purpose of this study was to see if Sym023 is safe and tolerable for patients with locally advanced/unresectable or metastatic solid tumor malignancies or lymphomas that are refractory to available therapy or for which no standard therapy is available.

Timeline

Start
2018-05-24
Primary completion
2020-06-03
Completion
2020-06-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Sym023 Monoclonal antibody 0.03 mg/kg Intravenous
Subject Sym023 Monoclonal antibody 0.1 mg/kg Intravenous
Subject Sym023 Monoclonal antibody 0.3 mg/kg Intravenous
Subject Sym023 Monoclonal antibody 1 mg/kg Intravenous
Subject Sym023 Monoclonal antibody 3 mg/kg Intravenous
Subject Sym023 Monoclonal antibody 10 mg/kg Intravenous
Subject Sym023 Monoclonal antibody 20 mg/kg Intravenous