drugset / Trial / NCT01561911

A Phase I Study of the Chimeric Anti-CD40 Monoclonal Antibody ChiLob 7/4 to Treat Advanced Malignancies Refractory to Conventional Anti-cancer Treatment

NCT01561911 ↗

Phase 1 Completed 29 enrolled Cancer Research UK
Open-label

Summary

The Purpose of this study is to evaluate the safety and tolerability, and the biological effects of the chimeric anti-CD40 monoclonal antibody Chi Lob 7/4, given intravenously, weekly for 4 weeks in the treatment of patients with advanced malignancies refractory to conventional anti-cancer treatment.

Timeline

Start
2007-07
Primary completion
2014-10
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject ChiLob7/4 Unknown 0.5 mg Intravenous
Subject ChiLob7/4 Unknown 1.6 mg Intravenous
Subject ChiLob7/4 Unknown 5 mg Intravenous
Subject ChiLob7/4 Unknown 16 mg Intravenous
Subject ChiLob7/4 Unknown 50 mg Intravenous
Subject ChiLob7/4 Unknown 160 mg Intravenous
Subject ChiLob7/4 Unknown 240 mg Intravenous
Subject ChiLob7/4 Unknown 320 mg Intravenous