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NCT01050790 · ClinicalTrials.gov registry record · NA

Lenalidomide + Azacitidine for Adaptive Immunotherapy -> Auto SCT in Multiple Myeloma

A NA study, sponsored by Virginia Commonwealth University.

Completed
Registry status
NA
Development phase
17
Enrollment target

NCT01050790: Completed NA study, sponsored by Virginia Commonwealth University.

NCT01050790 is a NA study that has completed, run by Virginia Commonwealth University. The registered enrollment target is 17 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01050790, a NA study, has completed, sponsored by Virginia Commonwealth University.

COMPLETED
Registry status
NA
Development phase
17 participants
Enrollment target

Study Summary

RATIONALE: Lenalidomide may stimulate the immune system in different ways and stop cancer cells from growing. Drugs used in chemotherapy, such as azacitidine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. An autologous stem cell transplant may be able to replace blood-forming cells that were destroyed by lenalidomide and azacitidine. Giving autologous lymphocytes after the transplant may help destroy any remaining cancer cells. PURPOSE: This pilot trial is studying how well giving lenalidomide together with azacitidine works when followed by autologous stem cell transplant and autologous lymphocyte infusion in treating patients with multiple myeloma.

Primary Outcome

Time frame is post 2nd and 3rd cycles of rev/aza and after stem cell transplant engraftment.

Interventions

  • DRUG Azacitidine

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2010-01
Est. Completion 2016-09
Phase NA
Virginia Commonwealth University

558 total trials

What the finished NCT01050790 record still lists

NCT01050790 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which Azacitidine is the first listed.

NCT01050790 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01050790 about?

NCT01050790 is a clinical study titled "Lenalidomide + Azacitidine for Adaptive Immunotherapy -> Auto SCT in Multiple Myeloma". RATIONALE: Lenalidomide may stimulate the immune system in different ways and stop cancer cells from growing. Drugs used in chemotherapy, such as azacitidine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. An autologous stem ...

What is the current status of trial NCT01050790?

This trial is currently completed. It is a NA study. The enrollment target is 17 participants. The study started on 2010-01. Estimated completion is 2016-09.

What interventions are being tested in trial NCT01050790?

The interventions under investigation include: Azacitidine (DRUG).

Who is sponsoring clinical trial NCT01050790?

This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01050790's enrollment target sits among peer trials

17 1871st of 2000 higher than 130 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT01050790, the US trial registry maintained by the National Library of Medicine. NCT01050790 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.