drugset / Trial / NCT03580564

An Open, Multicenter Phase II Study to Evaluate the Safety and Efficacy of KL-A167 Injection in Relapsed or Refractory Classical Hodgkin's Lymphoma

NCT03580564

Phase 2 Completed 109 enrolled Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The study is to evaluate the efficacy of KL-A167 a in subjects with relapsed or refractory classical Hodgkin lymphoma (cHL), as measured by Overall Response Rate (ORR) per the Lugano Classification

Timeline

Start
2018-08-01
Primary completion
2020-08-22
Completion
2022-01-13

Drugs

EvaluationDrugModalityDoseRoute
Subject KL-A167 Unknown 900 mg Intravenous