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Clinical Trial Summary

The work proposed herein aims to provide the first prospective, randomized comparative efficacy data between Melphalan and BEAM treatment regimen in the Multiple Myeloma (MM) patient population. The risk of such a study is deemed reasonable and ethical since: a) previous works have closely examined the safety and toxicity of the BEAM regimen and the doses to be delivered in this protocol are well below the toxicity levels; b) phase III trials of BEAM have provided reasonable data regarding the efficacy in lymphomas c) Early, retrospective data suggests that BEAM may be efficacious in MM however due to the lack of prospective controlled randomized clinical trial, there is adequate equipoise regarding its efficacy and moreover its comparative efficacy in relation to Melphalan and; D) there are known limitations in the standard-of-care for MM, Melphalan, namely, relatively low rates of complete response at the time of Autologous stem-cell transplantation (ASCT) and poor progression free survival.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03570983
Study type Interventional
Source Swedish Medical Center
Contact Janell Duey, JD
Phone 206-386-2572
Email Janell.Duey@swedish.org
Status Recruiting
Phase Phase 2
Start date September 5, 2018
Completion date December 2021

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