drugset / Trial / NCT00899847
Phase 2 Study of Autologous Followed by Nonmyeloablative Allogeneic Transplantation Using TLI & ATG
NaSingle-groupOpen-labelTreatment
Summary
To evaluate the toxicity and tolerability of this tandem autologous/allogeneic transplant approach for patients with advanced stage multiple myeloma.
Timeline
- Start
- 2009-05
- Primary completion
- 2014-04
- Completion
- 2014-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Background | Acetaminophen | Small molecule | 650 mg | — |
| Background | Cyclophosphamide | Other / unclassified | 4 g | Intravenous |
| Background | Cyclosporine | Peptide | 5 mg/kg | Oral |
| Background | Diphenhydramine | Unknown | 25 mg | — |
| Background | Diphenhydramine | Unknown | 50 mg | — |
| Background | Hydrocortisone | Other / unclassified | 100 mg | Intravenous |
| Background | Melphalan | Small molecule | 200 mg/m2 | Intravenous |
| Background | Methylprednisolone | Other / unclassified | 1 mg/kg | Intravenous |
| Background | Mycophenolate Mofetil | Small molecule | 15 mg/kg | Oral |
| Background | Thymoglobulin | Protein / enzyme biologic | 1.5 mg/kg | Intravenous |
| Background | filgrastim | Protein / enzyme biologic | 5 ug/kg | Subcutaneous |
| Background | filgrastim | Protein / enzyme biologic | 10 ug/kg | Subcutaneous |
| Background | filgrastim | Protein / enzyme biologic | 16 ug/kg | Subcutaneous |