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NCT00807599 · ClinicalTrials.gov registry record · Phase 2

Lenalidomide (Revlimid®) Plus Low-dose Dexamethasone (Ld x 4 Cycles) Then Stem Cell Collection Followed by Randomization to Continued Ld or Stem Cell Transplantation (SCT) Plus Maintenance L

A Phase 2 study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 2
Development phase
67
Enrollment target

NCT00807599: Completed Phase 2 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT00807599 is a Phase 2 study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 67 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00807599, a Phase 2 study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
67 participants
Enrollment target

Study Summary

The purpose of this study is to compare the effects, good and bad, of two ways to treat patients with standard-risk symptomatic multiple myeloma. Patients with standard-risk myeloma have myeloma with specific features: levels of 2 blood tests have to be in a specific range and there can be no myeloma tumors found outside of the bones or bone marrow, the areas where myeloma is usually discovered. In past clinical studies, patients with standard-risk myeloma have done well with intensive therapy in the form of stem cell transplant. But multiple myeloma is not curable and, although it may respond to standard treatments including stem cell transplant, myeloma always recurs.

Interventions

  • PROCEDURE Stem cell transplant x 1 or x 2
  • DRUG lenalidomide and dexamethasone

Trial Details

FieldValue
Enrollment Target 67 participants
Start Date 2008-12-10
Est. Completion 2018-07
Phase Phase 2

Sponsor

Memorial Sloan Kettering Cancer Center

1,884 total trials

What the Registry Record Tells You About NCT00807599

The ClinicalTrials.gov registry entry for NCT00807599 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 67 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 1,884 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Stem cell transplant x 1 or x 2 is the first listed.

NCT00807599 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00807599 about?

NCT00807599 is a clinical study titled "Lenalidomide (Revlimid®) Plus Low-dose Dexamethasone (Ld x 4 Cycles) Then Stem Cell Collection Followed by Randomization to Continued Ld or Stem Cell Transplantation (SCT) Plus Maintenance L". The purpose of this study is to compare the effects, good and bad, of two ways to treat patients with standard-risk symptomatic multiple myeloma. Patients with standard-risk myeloma have myeloma with specific features: levels of 2 blood tests have to be in a specific range and there can be no myelom...

What is the current status of trial NCT00807599?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 67 participants. The study started on 2008-12-10. Estimated completion is 2018-07.

What interventions are being tested in trial NCT00807599?

The interventions under investigation include: Stem cell transplant x 1 or x 2 (PROCEDURE), lenalidomide and dexamethasone (DRUG).

Who is sponsoring clinical trial NCT00807599?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.