drugset / Trial / NCT02013804
A Phase 1 Multicenter Open-label Study to Evaluate the Safety Tolerability and PK of MEDI0680 (AMP-514) in Subjects With Advanced Malignancies
NaSingle-groupOpen-labelTreatment
Summary
This is a multicenter, open label, first-in-human dose-escalation study of MEDI0680 (AMP-514) to evaluate the safety, tolerability, PK, immunogenicity (IM), and antitumor activity in adult subjects with solid tumors.
Timeline
- Start
- 2013-12-19
- Primary completion
- 2017-05-18
- Completion
- 2017-05-18
Publications
- Naing A, Infante J, Goel S, Burris H, Black C, Marshall S, Achour I, Barbee S, May R, Morehouse C, Pollizzi K, Song X, Steele K, Elgeioushi N, Walcott F, Karakunnel J, LoRusso P, Weise A, Eder J, Curti B, Oberst M. Anti-PD-1 monoclonal antibody MEDI0680 in a phase I study of patients with advanced solid malignancies. J Immunother Cancer. 2019 Aug 22;7(1):225. doi: 10.1186/s40425-019-0665-2.
- Borch TH, Donia M, Andersen MH, Svane IM. Reorienting the immune system in the treatment of cancer by using anti-PD-1 and anti-PD-L1 antibodies. Drug Discov Today. 2015 Sep;20(9):1127-34. doi: 10.1016/j.drudis.2015.07.003. Epub 2015 Jul 17.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MEDI0680 | Monoclonal antibody | 0.1 mg/kg | Intravenous |
| Subject | MEDI0680 | Monoclonal antibody | 0.5 mg/kg | Intravenous |
| Subject | MEDI0680 | Monoclonal antibody | 2.5 mg/kg | Intravenous |
| Subject | MEDI0680 | Monoclonal antibody | 10 mg/kg | Intravenous |
| Subject | MEDI0680 | Monoclonal antibody | 20 mg/kg | Intravenous |