drugset / Trial / NCT02432235

Study of ADCT-301 in Patients With Relapsed or Refractory Hodgkin and Non-Hodgkin Lymphoma

NCT02432235 ↗

Phase 1 Completed 133 enrolled ADC Therapeutics S.A.
Non-randomizedSequentialOpen-labelTreatment

Summary

This study evaluates camidanlumab tesirine in participants with relapsed/refractory Non-Hodgkin or Hodgkin lymphoma.

Timeline

Start
2015-10-05
Primary completion
2019-10-24
Completion
2019-10-24

Drugs

EvaluationDrugModalityDoseRoute
Subject ADCT-301 Monoclonal antibody 3 ug/kg Intravenous
Subject ADCT-301 Monoclonal antibody 5 ug/kg Intravenous
Subject ADCT-301 Monoclonal antibody 8 ug/kg Intravenous
Subject ADCT-301 Monoclonal antibody 13 ug/kg Intravenous
Subject ADCT-301 Monoclonal antibody 20 ug/kg Intravenous
Subject ADCT-301 Monoclonal antibody 30 ug/kg Intravenous
Subject ADCT-301 Monoclonal antibody 45 ug/kg Intravenous
Subject ADCT-301 Monoclonal antibody 60 ug/kg Intravenous
Subject ADCT-301 Monoclonal antibody 80 ug/kg Intravenous
Subject ADCT-301 Monoclonal antibody 100 ug/kg Intravenous
Subject ADCT-301 Monoclonal antibody 150 ug/kg Intravenous