drugset / Trial / NCT00785538
A Study of IMC-A12 in Participants With Tumors Who No Longer Respond to Treatment or For Whom No Treatment is Available
SequentialOpen-labelTreatment
Summary
The purpose of this study is to determine if IMC-A12 is safe for participants, and also to determine the best dose of IMC-A12 to give to participants.
Timeline
- Start
- 2005-10
- Primary completion
- 2011-01
- Completion
- 2011-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Cixutumumab | Monoclonal antibody | 3 mg/kg | Intravenous |
| Subject | Cixutumumab | Monoclonal antibody | 6 mg/kg | Intravenous |
| Subject | Cixutumumab | Monoclonal antibody | 10 mg/kg | Intravenous |
| Subject | Cixutumumab | Monoclonal antibody | 15 mg/kg | Intravenous |
| Subject | Cixutumumab | Monoclonal antibody | 21 mg/kg | Intravenous |
| Subject | Cixutumumab | Monoclonal antibody | 27 mg/kg | Intravenous |