drugset / Trial / NCT04819399

Investigation of Safety and Tolerability of Catumaxomab in Patients With NMIBC

NCT04819399 ↗

Phase 1 Unknown 30 enrolled Lindis Biotech GmbH
NaSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to investigate the safety, tolerability, and preliminary efficacy of the monoclonal bispecific trifunctional antibody Catumaxomab in patients with non-muscle invasive bladder cancer (NMIBC).

Timeline

Start
2020-07-07
Primary completion
2022-12-30
Completion
2023-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Catumaxomab Monoclonal antibody 50 ug Other
Subject Catumaxomab Monoclonal antibody 70 ug Other
Subject Catumaxomab Monoclonal antibody 100 ug Other