drugset / Trial / NCT00899847

Phase 2 Study of Autologous Followed by Nonmyeloablative Allogeneic Transplantation Using TLI & ATG

NCT00899847

Phase 2 Completed 9 enrolled Stanford University
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

EvaluationDrugModalityDoseRoute
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

Indications