Bortezomib-Melphalan
DrugBortezomib will be administered on days: -6, -3, +1, +4. Melphalan will be administered on day -2. The PBSC will be injected on day 0.
NCT Number: NCT02197221
Phase III multicenter randomized, open-label study comparing the efficacy of a combined high dose chemotherapy using melphalan and bortezomib versus melphalan alone followed by stem cell transplant in frontline multiple myeloma patients, non-progressive after induction therapy.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 3
Clinique Universitaire Saint Luc, Brussels, Belgium
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Bortezomib will be administered on days: -6, -3, +1, +4. Melphalan will be administered on day -2. The PBSC will be injected on day 0.
Melphalan will be administered on day -2. The PBSC will be injected on day 0.
Time frame: 60 days post Autologous Stem Cells Transplantation
Time frame: 60 months
Time frame: post ASCT and consolidation therapy
Compare response rate after ASCT and after the completion of consolidation therapy
Time frame: End of study
Time frame: 60 months
University Hospital, Toulouse
Other
IFM 2014-02 Study: A Randomized Phase III Study of Bortezomib-Melphalan 200 Conditioning Regimen Versus Melphalan 200 for Frontline Transplant Eligible Patients With Multiple Myeloma
Acronym: IFM2014-02
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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