CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 71 enrolled
Drug / intervention
busulfan +2 moredrug
Likely dose
busulfan 0.8 mg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00941720
NCT00941720Phase 2Completed

A Study of Outcomes and Toxicity of Busulfex as Part of a High Dose Chemotherapy Preparative Regimen in Autologous Hematopoietic Stem Cell Transplantation for Patients With Plasma Cell Myeloma

Case Comprehensive Cancer Center·interventional·Posted Jul 20, 2009·Updated Jul 24, 2020

In Brief

A Phase 2 clinical trial evaluating busulfan, cyclophosphamide, and 1 other intervention for Multiple Myeloma and Plasma Cell Neoplasm. Completed, enrolled 71 participants across 1 site.

Detailed Summary

RATIONALE: Giving high-dose chemotherapy before an autologous stem cell transplant stops the growth of cancer cells by stopping them from dividing or killing them. An autologous stem cell transplant may be able to replace the blood-forming cells that were destroyed by the chemotherapy. PURPOSE: This phase II trial is studying how well giving busulfan together with cyclophosphamide followed by an autologous stem cell transplant works in treating patients with multiple myeloma.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedJul 20, 2009
Enrollment StartJun 11, 2009
Primary CompletionFeb 28, 2013
TodayJul 2, 2026
Enrollment to primary: 3.7 yearsPosted 16.9 years ago

Interventions

busulfandrug

IV busulfan 0.8 mg/kg every 6 hours x 16 doses

cyclophosphamidedrug

IV cyclophosphamide 60 mg/kg over 4 hours x 2 days

autologous hematopoietic stem cell transplantationprocedure

infusion of autologous hematopoietic stem cells of at least 2.0 x 106 CD34+ cells/kg on day 0