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NCT01653418 · ClinicalTrials.gov registry record · Phase 2

Phase II Study of V-BEAM Conditioning Regimen Prior to Second Autologous Stem Cell Transplantation

A Phase 2 study, sponsored by Washington University School of Medicine.

Terminated
Registry status
Phase 2
Development phase
10
Enrollment target

NCT01653418: Clinical Trial Phase 2 study, sponsored by Washington University School of Medicine.

NCT01653418 is a Phase 2 study that was terminated before completion, run by Washington University School of Medicine. The registered enrollment target is 10 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01653418, a Phase 2 study, was terminated before completion, sponsored by Washington University School of Medicine.

TERMINATED
Registry status
Phase 2
Development phase
10 participants
Enrollment target

Study Summary

BEAM regimen (BCNU, etoposide, cytarabine, and melphalan) is the most commonly used conditioning regimen for relapsed/refractory lymphoma patients needing autologous stem cell transplantation. Since these components are all effective in myeloma and bortezomib has shown promising results in the transplant setting, here the investigators propose a phase II study to investigate the combination of bortezomib and BEAM as a new conditioning regimen for patients who relapse or progress after the first autologous transplantation and for whom a second autologous transplant is considered.

Primary Outcome

Defined by the International Myeloma Working Group (IMWG) criteria

Interventions

  • DRUG Melphalan
  • DRUG Etoposide
  • DRUG Cytarabine
  • DRUG Carmustine
  • DRUG Bortezomib

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2012-09
Est. Completion 2013-12
Phase Phase 2

Why NCT01653418 stopped before completion

NCT01653418 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 5 interventions - of which Melphalan is the first listed.

NCT01653418 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01653418 about?

NCT01653418 is a clinical study titled "Phase II Study of V-BEAM Conditioning Regimen Prior to Second Autologous Stem Cell Transplantation". BEAM regimen (BCNU, etoposide, cytarabine, and melphalan) is the most commonly used conditioning regimen for relapsed/refractory lymphoma patients needing autologous stem cell transplantation. Since these components are all effective in myeloma and bortezomib has shown promising results in the trans...

What is the current status of trial NCT01653418?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 10 participants. The study started on 2012-09. Estimated completion is 2013-12.

What interventions are being tested in trial NCT01653418?

The interventions under investigation include: Melphalan (DRUG), Etoposide (DRUG), Cytarabine (DRUG), Carmustine (DRUG), Bortezomib (DRUG).

Who is sponsoring clinical trial NCT01653418?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01653418's enrollment target sits among peer trials

10 1968th of 2000 higher than 12 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01653418, the US trial registry maintained by the National Library of Medicine. NCT01653418 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.