drugset / Trial / NCT01504256

Catumaxomab for Treatment of Peritoneal Carcinomatosis in Patients With Gastric Adenocarcinomas

NCT01504256 ↗

Phase 2 Completed 42 enrolled AIO-Studien-gGmbH Neovii Biotech · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the efficacy of catumaxomab by determination of the rate of macroscopic complete remissions of peritoneal carcinomatosis after treatment with one cycle (four doses) of catumaxomab followed by six cycles of routine neoadjuvant chemotherapy.

Timeline

Start
2011-10
Primary completion
2017-03
Completion
2017-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Catumaxomab Monoclonal antibody 150 ug Other
Background Docetaxel Small molecule 50 mg/m2 —
Background Leucovorin Small molecule 200 mg/m2 —
Background Oxaliplatin Small molecule 85 mg/m2 —
Background fluorouracil Small molecule 2600 mg/m2 —