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NCT01056276 · ClinicalTrials.gov registry record · Phase 2

Study to Evaluate the Combination of Bendamustine, Bortezomib and Dexamethasone (BBD) in the First-Line Treatment of Patients With Multiple Myeloma Who Are Not Candidates for High Dose Chemotherapy

A Phase 2 study, sponsored by SCRI Development Innovations.

Completed
Registry status
Phase 2
Development phase
59
Enrollment target

NCT01056276: Completed Phase 2 study, sponsored by SCRI Development Innovations.

NCT01056276 is a Phase 2 study that has completed, run by SCRI Development Innovations. The registered enrollment target is 59 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (56% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01056276, a Phase 2 study, has completed, sponsored by SCRI Development Innovations.

COMPLETED
Registry status
Phase 2
Development phase
59 participants
Enrollment target

Study Summary

In this study, investigators will evaluate the activity of bendamustine, bortezomib and dexamethasone (BBD). This regimen combines 3 agents with high activity in multiple myeloma, with different mechanisms of action and non-overlapping toxicities.

Primary Outcome

Defined as the percent of patients having a complete response (CR) to treatment, assessed using the International Myeloma Working Group (IMWG) Uniform Response Criteria. CR=disappearance of soft tissue plasmacytomas and 5% or less plasma cells in bone marrow.

Interventions

  • DRUG Dexamethasone
  • DRUG Bendamustine
  • DRUG Bortezomib

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2010-05
Est. Completion 2017-02
Phase Phase 2
SCRI Development Innovations

146 total trials

What the finished NCT01056276 record still lists

NCT01056276 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 59 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (56% lower).

The record links to 0 conditions, and to 3 interventions - of which Dexamethasone is the first listed.

NCT01056276 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01056276 about?

NCT01056276 is a clinical study titled "Study to Evaluate the Combination of Bendamustine, Bortezomib and Dexamethasone (BBD) in the First-Line Treatment of Patients With Multiple Myeloma Who Are Not Candidates for High Dose Chemotherapy". In this study, investigators will evaluate the activity of bendamustine, bortezomib and dexamethasone (BBD). This regimen combines 3 agents with high activity in multiple myeloma, with different mechanisms of action and non-overlapping toxicities.

What is the current status of trial NCT01056276?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 59 participants. The study started on 2010-05. Estimated completion is 2017-02.

What interventions are being tested in trial NCT01056276?

The interventions under investigation include: Dexamethasone (DRUG), Bendamustine (DRUG), Bortezomib (DRUG).

Who is sponsoring clinical trial NCT01056276?

This trial is sponsored by SCRI Development Innovations, which has 146 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01056276's enrollment target sits among peer trials

59 1133rd of 2000 higher than 866 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 NCT01056276, the US trial registry maintained by the National Library of Medicine. NCT01056276 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.