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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |