drugset / Trial / NCT05216835

Safety and Preliminary Efficacy Assessment of AZD7789 in Patients With Relapsed or Refractory Classical Hodgkin Lymphoma

NCT05216835

Phase 1 Completed 45 enrolled AstraZeneca Parexel · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

The study is intended to assess the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of sabestomig (AZD7789) in patients with relapsed/refractory classical Hodgkin Lymphoma (r/r cHL).

Timeline

Start
2022-03-18
Primary completion
2024-08-30
Completion
2025-09-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Sabestomig Monoclonal antibody Intravenous