drugset / Trial / NCT02204046

Biodistribution Study With 186 Re-labelled Humanised Monoclonal Antibody BIWA 4 in Patients With Adenocarcinoma of the Breast

NCT02204046 ↗

Phase 1 Completed 9 enrolled Boehringer Ingelheim
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The primary objectives of this study were to assess the safety and tolerability of intravenously (i.v.) administered 186Rhenium (186Re)-labelled bivatuzumab and to investigate the biodistribution and pharmacokinetics of 186Re-labelled bivatuzumab in patients with adenocarcinoma of the breast

Timeline

Start
2000-01
Primary completion
2001-02
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject Bivatuzumab Monoclonal antibody — Intravenous

Indications