drugset / Trial / NCT00102024

Safety and Activity of 90Y-Labeled IDEC-159 in Subjects With Metastatic Colorectal Adenocarcinoma

NCT00102024 ↗

Phase 1/2 Terminated 30 enrolled Biogen
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is a Phase I/II open-label, dose-escalating study in patients with metastatic colorectal cancer. The objectives of the study are to obtain information on the safety of radiolabeled IDEC-159, as well as its activity in colorectal cancer. Another objective is to determine the maximum tolerated dose (MTD). The study duration is 2 years with visits occuring daily and/or weekly for the first 3 months, and every 6 weeks until the end of the 2 year period.

Timeline

Start
2005-01
Primary completion
2006-01
Completion
2006-01

Drugs

EvaluationDrugModalityDoseRoute
Subject 111In-IDEC-159 Unknown — —
Subject 90Y-IDEC-159 Monoclonal antibody — —
Background IDEC-159 Monoclonal antibody — —