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An Open-Label, Dose-Finding Study to Evaluate the Safety of AMG 706 Plus Panitumumab Plus Gemcitabine-Cisplatin in the Treatment of Subjects With Advanced Cancer
The purpose of this study is to characterize the safety and tolerability of AMG 706 plus panitumumab when administered with gemcitabine and cisplatin chemotherapy. This is a Phase 1b clinical study.
Details
| Lead sponsor | Amgen |
|---|---|
| Phase | Phase 1 |
| Status | TERMINATED |
| Enrolment | 41 |
| Start date | 2004-12 |
| Completion | 2008-04 |
Conditions
- Lung Cancer
- Pancreatic Cancer
- Esophageal Cancer
Interventions
- AMG 706
- Panitumumab
- Gemcitabine
- Cisplatin
Primary outcomes
- Participant Incidence of Adverse Events — From the first dose of any study treatment until 30 days after the last dose of study treatment, up to a maximum of 509 days.
The number of participants who experienced at least one treatment-emergent adverse event. Additional details regarding specfic adverse events are provided in the Adverse Event section of this posting.