drugset / Trial / NCT01413178

A Randomized Trial to Compare Busulfan + Melphalan 140 mg/m2 With Melphalan 200 mg/m2 as Preparative Regimen for Autologous Hematopoietic Stem Cell Transplantation for Multiple Myeloma

NCT01413178 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

The goal of this clinical research study is to compare Busulfex (busulfan) with or without Alkeran (melphalan) to learn which study therapy may be better at helping to control MM in patients who will receive an autologous stem cell transplant. The safety of this combination therapy will also be studied. Melphalan and busulfan are designed to damage the DNA (genetic material) of cells, which may cause cancer cells to die.

Timeline

Start
2011-09-30
Primary completion
2019-03-10
Completion
2019-03-10

Outcome

Met primary endpoint

paper 64·7 months (32·9-64·7) with busulfan plus melphalan versus 43·5 months (19·9-not estimated) with melphalan alone (hazard ratio 0·53 [95% CI 0·30-0·91]; p=0·022). PMID 30910541 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Busulfan Small molecule 130 mg/m2 Intravenous
Subject Melphalan Small molecule 70 mg/m2 Intravenous
Subject Melphalan Small molecule 200 mg/m2 Intravenous
Background G-CSF Unknown 5 ug/kg Subcutaneous

Indications