drugset / Trial / NCT01409343

TrasGEX™: Phase 1 Study in Cancer Patients

NCT01409343 ↗

NaSingle-groupOpen-labelTreatment

Summary

This was a prospective, open label, multicenter study evaluating the safety, tolerability and pharmacokinetics of TrasGEX™ after intravenous administration in patients with HER-2 positive cancers. The effect of TrasGEX™ on the development of anti-drug antibodies and on tumour response was also evaluated.

Timeline

Start
2011-07
Primary completion
2013-11
Completion
2013-12

Drugs

EvaluationDrugModalityDoseRoute
Subject TrasGEX Monoclonal antibody 12 mg Intravenous
Subject TrasGEX Monoclonal antibody 720 mg Intravenous

Indications