drugset / Trial / NCT00303472
Determination of Safe Dose of Romiplostim (AMG 531) in Patients With Myelodysplastic Syndromes (MDS)
Non-randomizedSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to evaluate the safety and tolerability of romiplostim in thrombocytopenic patients with low or Intermediate-1 risk MDS. In addition, the study will evaluate the platelet response to romiplostim.
Timeline
- Start
- 2006-02
- Primary completion
- 2008-05
- Completion
- 2008-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Romiplostim | Peptide | 300 ug | Subcutaneous |
| Subject | Romiplostim | Peptide | 700 ug | Subcutaneous |
| Subject | Romiplostim | Peptide | 750 ug | Subcutaneous |
| Subject | Romiplostim | Peptide | 1000 ug | Subcutaneous |
| Subject | Romiplostim | Peptide | 1500 ug | Subcutaneous |