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NCT00166413 · ClinicalTrials.gov registry record · Phase 2

Efficacy of CC-5013 (Revlimid or Lenalidomide) in Patients With Primary Systemic Amyloidosis

A Phase 2 study, sponsored by Mayo Clinic.

Completed
Registry status
Phase 2
Development phase
38
Enrollment target

NCT00166413: Completed Phase 2 study, sponsored by Mayo Clinic.

NCT00166413 is a Phase 2 study that has completed, run by Mayo Clinic. The registered enrollment target is 38 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (71% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00166413, a Phase 2 study, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
Phase 2
Development phase
38 participants
Enrollment target

Study Summary

Patients with primary systemic amyloidosis will be treated with CC-5013 (lenalidomide; Revlimid) as a single agent for 3 months. If their disease worsens or does not improve during that time frame dexamethasone will be added to the treatment program.

Interventions

  • DRUG CC-5013

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2005-04
Phase Phase 2
Mayo Clinic

2,844 total trials

What the finished NCT00166413 record still lists

NCT00166413 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 38 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (71% lower).

The record links to 0 conditions, and to 1 intervention - of which CC-5013 is the first listed.

NCT00166413 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00166413 about?

NCT00166413 is a clinical study titled "Efficacy of CC-5013 (Revlimid or Lenalidomide) in Patients With Primary Systemic Amyloidosis". Patients with primary systemic amyloidosis will be treated with CC-5013 (lenalidomide; Revlimid) as a single agent for 3 months. If their disease worsens or does not improve during that time frame dexamethasone will be added to the treatment program.

What is the current status of trial NCT00166413?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 38 participants. The study started on 2005-04.

What interventions are being tested in trial NCT00166413?

The interventions under investigation include: CC-5013 (DRUG).

Who is sponsoring clinical trial NCT00166413?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00166413's enrollment target sits among peer trials

38 1467th of 2000 higher than 517 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 NCT00166413, the US trial registry maintained by the National Library of Medicine. NCT00166413 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.